Pediatric-Neonatal Perinatal CME
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Pediatric-Neonatal Perinatal Articles (398)
Featured Activities
Pediatric-Neonatal Perinatal Activities
| Title | Description | Hours | Questions | |
|---|---|---|---|---|
| 21 Hydroxylase Deficiency | 21-hydroxylase deficiency is an autosomal recessive disorder caused by a deficiency in one of the enzymes required for the synthesis of cortisol in th ... Read the Article | 1 | 4 | Activity DO |
| 21 Hydroxylase Deficiency | 21-hydroxylase deficiency is an autosomal recessive disorder caused by a deficiency in one of the enzymes required for the synthesis of cortisol in th ... Read the Article | 1 | 4 | Activity MD/PA |
| Abnormal Neonatal EEG | Electroencephalogram of a newborn shows unique features compared to older children and adults. The principles employed in the identification of abnorm ... Read the Article | 1 | 5 | Activity DO |
| Abnormal Neonatal EEG | Electroencephalogram of a newborn shows unique features compared to older children and adults. The principles employed in the identification of abnorm ... Read the Article | 1 | 5 | Activity MD/PA |
| Achondroplasia | Achondroplasia is the most common skeletal dysplasia found in humans, accounting for 90% of cases of disproportionate short stature. It is caused by a ... Read the Article | 1.5 | 13 | Activity DO |
| Achondroplasia | Achondroplasia is the most common skeletal dysplasia found in humans, accounting for 90% of cases of disproportionate short stature. It is caused by a ... Read the Article | 1.5 | 13 | Activity MD/PA |
| Acrodermatitis Enteropathica | Acrodermatitis enteropathica is a rare skin disorder associated with zinc deficiency that is most often seen in infants. Zinc is a very important micr ... Read the Article | 1 | 7 | Activity DO |
| Acrodermatitis Enteropathica | Acrodermatitis enteropathica is a rare skin disorder associated with zinc deficiency that is most often seen in infants. Zinc is a very important micr ... Read the Article | 1 | 7 | Activity MD/PA |
| Acute Myeloid Leukemia | Acute myeloid leukemia (AML) is the most common leukemia among the adult population and accounts for about 80% of all cases. It is characterized by cl ... Read the Article | 1.25 | 10 | Activity DO |
| Acute Myeloid Leukemia | Acute myeloid leukemia (AML) is the most common leukemia among the adult population and accounts for about 80% of all cases. It is characterized by cl ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Adrenal Hypoplasia | Adrenal hypoplasia is a condition in which there is underdevelopment or hypotrophy of the adrenal cortex due to several clinical conditions. It falls ... Read the Article | 1 | 5 | Activity DO |
| Adrenal Hypoplasia | Adrenal hypoplasia is a condition in which there is underdevelopment or hypotrophy of the adrenal cortex due to several clinical conditions. It falls ... Read the Article | 1 | 5 | Activity MD/PA |
| Adrenoleukodystrophy | Adrenoleukodystrophy is a peroxisomal disorder resulting from abnormal metabolism of the very-long-chain fatty acids (VLCFA). It is classified into di ... Read the Article | 1.25 | 13 | Activity DO |
| Adrenoleukodystrophy | Adrenoleukodystrophy is a peroxisomal disorder resulting from abnormal metabolism of the very-long-chain fatty acids (VLCFA). It is classified into di ... Read the Article | 1.25 | 13 | Activity MD/PA |
| Agammaglobulinemia | Agammaglobulinemia or hypogammaglobulinemia is a rare inherited immunodeficiency disorder, characterized by low or absent B cells with absent immunogl ... Read the Article | 1.25 | 8 | Activity DO |
| Agammaglobulinemia | Agammaglobulinemia or hypogammaglobulinemia is a rare inherited immunodeficiency disorder, characterized by low or absent B cells with absent immunogl ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Airway Obstruction | Airway obstruction secondary to a foreign body is often easily treated, as the foreign body can be removed, and the patency of the airway restored. Ho ... Read the Article | 1 | 4 | Activity DO |
| Airway Obstruction | Airway obstruction secondary to a foreign body is often easily treated, as the foreign body can be removed, and the patency of the airway restored. Ho ... Read the Article | 1 | 4 | Activity MD/PA |
| Airway Suctioning | Airway suctioning is a procedure routinely performed in inpatient and outpatient settings. It is important to maintain the patency of the natural or a ... Read the Article | 1 | 6 | Activity DO |
| Airway Suctioning | Airway suctioning is a procedure routinely performed in inpatient and outpatient settings. It is important to maintain the patency of the natural or a ... Read the Article | 1 | 6 | Activity MD/PA |
| Akinesia | Akinesia or "absent movement" is a clinical sign that could be indicative of a number of disorders, depending on the age group of the patient. The var ... Read the Article | 1 | 5 | Activity DO |
| Akinesia | Akinesia or "absent movement" is a clinical sign that could be indicative of a number of disorders, depending on the age group of the patient. The var ... Read the Article | 1 | 5 | Activity MD/PA |
| Alagille Syndrome | Alagille syndrome (ALGS) is a multisystem autosomal dominant disorder with a wide variety of clinical manifestations. It is also known as arteriohepat ... Read the Article | 1 | 6 | Activity DO |
| Alagille Syndrome | Alagille syndrome (ALGS) is a multisystem autosomal dominant disorder with a wide variety of clinical manifestations. It is also known as arteriohepat ... Read the Article | 1 | 6 | Activity MD/PA |
| Alprostadil | Alprostadil is a medication used in the management and treatment of erectile dysfunction in males and for temporary patency of ductus arteriosus in ne ... Read the Article | 1 | 5 | Activity DO |
| Alprostadil | Alprostadil is a medication used in the management and treatment of erectile dysfunction in males and for temporary patency of ductus arteriosus in ne ... Read the Article | 1 | 5 | Activity MD/PA |
| Ambiguous Genitalia And Disorders of Sexual Differentiation | Infants born with a disorder of sex development (DSD) prompt multiple medical, surgical, ethical, psychosocial, and physical issues for patients and t ... Read the Article | 1.25 | 7 | Activity DO |
| Ambiguous Genitalia And Disorders of Sexual Differentiation | Infants born with a disorder of sex development (DSD) prompt multiple medical, surgical, ethical, psychosocial, and physical issues for patients and t ... Read the Article | 1.25 | 7 | Activity MD/PA |
| Amniotic Band Syndrome | Amniotic band syndrome (ABS) comprises various congenital anomalies, which include disruption, deformation, and malformations of organs that were inte ... Read the Article | 1 | 6 | Activity DO |
| Amniotic Band Syndrome | Amniotic band syndrome (ABS) comprises various congenital anomalies, which include disruption, deformation, and malformations of organs that were inte ... Read the Article | 1 | 6 | Activity MD/PA |
| Amniotic Fluid Embolism | Amniotic fluid embolism (AFE) is a rare entity, but one which has very high mortality and morbidity rates. This article will explain the clinical pres ... Read the Article | 1.25 | 9 | Activity DO |
| Amniotic Fluid Embolism | Amniotic fluid embolism (AFE) is a rare entity, but one which has very high mortality and morbidity rates. This article will explain the clinical pres ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Anesthesia For Patients With Myasthenia Gravis | Myasthenia Gravis is a neuromuscular disorder affecting muscarinic, nicotinic acetylcholine receptors. It is a disease characterized by weakness and f ... Read the Article | 1 | 5 | Activity DO |
| Anesthesia For Patients With Myasthenia Gravis | Myasthenia Gravis is a neuromuscular disorder affecting muscarinic, nicotinic acetylcholine receptors. It is a disease characterized by weakness and f ... Read the Article | 1 | 5 | Activity MD/PA |
| Anesthetic Considerations In Congenital Diaphragmatic Hernia | Congenital diaphragmatic herniation results in unique pathophysiologic changes that may prove to be a challenge to manage perioperatively. Anesthesiol ... Read the Article | 1 | 5 | Activity DO |
| Anesthetic Considerations In Congenital Diaphragmatic Hernia | Congenital diaphragmatic herniation results in unique pathophysiologic changes that may prove to be a challenge to manage perioperatively. Anesthesiol ... Read the Article | 1 | 5 | Activity MD/PA |
| Anesthetic Management Of Ex Utero Intrapartum Treatment (EXIT) And Fetal Surgery | In recent years, the significant advancement in imaging techniques has led to the early and detailed diagnoses of fetal abnormalities in utero. Some o ... Read the Article | 1 | 5 | Activity DO |
| Anesthetic Management Of Ex Utero Intrapartum Treatment (EXIT) And Fetal Surgery | In recent years, the significant advancement in imaging techniques has led to the early and detailed diagnoses of fetal abnormalities in utero. Some o ... Read the Article | 1 | 5 | Activity MD/PA |
| Anhidrosis | Anhidrosis is the inability to sweat. It is important to recognize anhidrosis as it can be potentially life-threatening due to heat-related illnesses. ... Read the Article | 1 | 5 | Activity DO |
| Anhidrosis | Anhidrosis is the inability to sweat. It is important to recognize anhidrosis as it can be potentially life-threatening due to heat-related illnesses. ... Read the Article | 1 | 5 | Activity MD/PA |
| Ankyloglossia | Ankyloglossia, also known as tongue-tie, is a short lingual frenum that interferes with normal tongue movement. It is an uncommon congenital oral anom ... Read the Article | 1.25 | 10 | Activity DO |
| Ankyloglossia | Ankyloglossia, also known as tongue-tie, is a short lingual frenum that interferes with normal tongue movement. It is an uncommon congenital oral anom ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Annular Pancreas | Annular pancreas (AP) is a rare congenital anomaly characterized by encasement of the duodenum by a band of pancreatic tissue. AP is not commonly enco ... Read the Article | 1 | 5 | Activity DO |
| Annular Pancreas | Annular pancreas (AP) is a rare congenital anomaly characterized by encasement of the duodenum by a band of pancreatic tissue. AP is not commonly enco ... Read the Article | 1 | 5 | Activity MD/PA |
| Antepartum Infections | This activity reviews the evaluation and management of antepartum infections and highlights the role of the interprofessional team in improving matern ... Read the Article | 1.25 | 8 | Activity DO |
| Antepartum Infections | This activity reviews the evaluation and management of antepartum infections and highlights the role of the interprofessional team in improving matern ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Antibody Deficiency Disorder | Antibody deficiency disorders may present soon after birth with recurrent infections. Normal individuals have 5 classes of immunoglobulins and several ... Read the Article | 1 | 4 | Activity DO |
| Antibody Deficiency Disorder | Antibody deficiency disorders may present soon after birth with recurrent infections. Normal individuals have 5 classes of immunoglobulins and several ... Read the Article | 1 | 4 | Activity MD/PA |
| Aortic Valvular Atresia | Aortic valvular atresia is a congenital condition in which the aortic valvular cusps are fused at birth. It frequently forms as a spectrum of malforma ... Read the Article | 1 | 5 | Activity DO |
| Aortic Valvular Atresia | Aortic valvular atresia is a congenital condition in which the aortic valvular cusps are fused at birth. It frequently forms as a spectrum of malforma ... Read the Article | 1 | 5 | Activity MD/PA |
| Aortopulmonary Septal Defect | An aortopulmonary or septal defect/aortopulmonary window is one of the rarest congenital heart defects. This defect develops embryologically when ther ... Read the Article | 1 | 7 | Activity DO |
| Aortopulmonary Septal Defect | An aortopulmonary or septal defect/aortopulmonary window is one of the rarest congenital heart defects. This defect develops embryologically when ther ... Read the Article | 1 | 7 | Activity MD/PA |
| Aortopulmonary Window | Aortopulmonary Window is a rare congenital cardiac malformation that can lead to congestive cardiac failure if left untreated. To avoid the high morbi ... Read the Article | 1 | 5 | Activity DO |
| Aortopulmonary Window | Aortopulmonary Window is a rare congenital cardiac malformation that can lead to congestive cardiac failure if left untreated. To avoid the high morbi ... Read the Article | 1 | 5 | Activity MD/PA |
| Aplasia Cutis Congenita | Aplasia cutis congenita (ACC) is a rare congenital skin defect characterized by a focal or extensive absence of the epidermis, dermis, and occasionall ... Read the Article | 1 | 5 | Activity DO |
| Aplasia Cutis Congenita | Aplasia cutis congenita (ACC) is a rare congenital skin defect characterized by a focal or extensive absence of the epidermis, dermis, and occasionall ... Read the Article | 1 | 5 | Activity MD/PA |
| Apnea In Children | Apnea can be defined as the cessation of respiratory effort lasting more than 20 seconds, or lasting a shorter duration but accompanied by bradycardia ... Read the Article | 1 | 7 | Activity DO |
| Apnea In Children | Apnea can be defined as the cessation of respiratory effort lasting more than 20 seconds, or lasting a shorter duration but accompanied by bradycardia ... Read the Article | 1 | 7 | Activity MD/PA |
| Arnold Chiari Malformation | Arnold-Chiari or Chiari malformations describe a group of deformities of the posterior fossa and hindbrain, which includes the cerebellum, pons, and m ... Read the Article | 1.25 | 10 | Activity DO |
| Arnold Chiari Malformation | Arnold-Chiari or Chiari malformations describe a group of deformities of the posterior fossa and hindbrain, which includes the cerebellum, pons, and m ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Atrial Septal Defect | Atrial septal defect (ASD) is one of the most common types of congenital heart defects, occurring in about 25% of children. An atrial septal defect oc ... Read the Article | 1.75 | 23 | Activity DO |
| Atrial Septal Defect | Atrial septal defect (ASD) is one of the most common types of congenital heart defects, occurring in about 25% of children. An atrial septal defect oc ... Read the Article | 1.75 | 23 | Activity MD/PA |
| Atrioventricular Septal Defect | The atrioventricular septal defect is a congenital cardiac malformation that is characterized by a variable degree of the atrial and ventricular septa ... Read the Article | 1.25 | 11 | Activity DO |
| Atrioventricular Septal Defect | The atrioventricular septal defect is a congenital cardiac malformation that is characterized by a variable degree of the atrial and ventricular septa ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Bacterial Conjunctivitis | Conjunctivitis, also informally known as "pink eye," makes up the majority of ophthalmologic disorders seen at primary care clinics. Patients present ... Read the Article | 1.25 | 8 | Activity DO |
| Bacterial Conjunctivitis | Conjunctivitis, also informally known as "pink eye," makes up the majority of ophthalmologic disorders seen at primary care clinics. Patients present ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Beckwith Wiedemann Syndrome | Beckwith-Wiedemann Syndrome is the most common overgrowth syndrome. It is a genetic imprinting disorder, and it can present as a wide and varied clini ... Read the Article | 1.25 | 8 | Activity DO |
| Beckwith Wiedemann Syndrome | Beckwith-Wiedemann Syndrome is the most common overgrowth syndrome. It is a genetic imprinting disorder, and it can present as a wide and varied clini ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Beta Thalassemia | Thalassemias are a common cause of microcytic anemia and are due to impaired synthesis of the globin protein component of hemoglobin. Beta-thalassemia ... Read the Article | 1.25 | 8 | Activity DO |
| Beta Thalassemia | Thalassemias are a common cause of microcytic anemia and are due to impaired synthesis of the globin protein component of hemoglobin. Beta-thalassemia ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Bilateral Vocal Cord Paralysis | Vocal cord paralysis refers to the immobility of a vocal cord, which can be due to pathology of the vocal ford (also known as the vocal fold) itself, ... Read the Article | 1 | 5 | Activity DO |
| Bilateral Vocal Cord Paralysis | Vocal cord paralysis refers to the immobility of a vocal cord, which can be due to pathology of the vocal ford (also known as the vocal fold) itself, ... Read the Article | 1 | 5 | Activity MD/PA |
| Biliary Atresia | Biliary atresia is a disease of the intrahepatic or extrahepatic bile ducts with an unknown etiology. It presents in neonates with jaundice, clay-colo ... Read the Article | 1 | 6 | Activity DO |
| Biliary Atresia | Biliary atresia is a disease of the intrahepatic or extrahepatic bile ducts with an unknown etiology. It presents in neonates with jaundice, clay-colo ... Read the Article | 1 | 6 | Activity MD/PA |
| Biotin Deficiency | Biotin is a B-complex vitamin that serves as an essential coenzyme for five carboxylases: pyruvate carboxylase, 3-methylcrotonyl-CoA carboxylase, prop ... Read the Article | 1 | 6 | Activity DO |
| Biotin Deficiency | Biotin is a B-complex vitamin that serves as an essential coenzyme for five carboxylases: pyruvate carboxylase, 3-methylcrotonyl-CoA carboxylase, prop ... Read the Article | 1 | 6 | Activity MD/PA |
| Biotinidase Deficiency | Biotin acts as a coenzyme for four carboxylation enzymes in the body: 3-methylcrontonyl-CoA carboxylase (MCC), pyruvate carboxylase (PC), acetyl-CoA c ... Read the Article | 1 | 4 | Activity DO |
| Biotinidase Deficiency | Biotin acts as a coenzyme for four carboxylation enzymes in the body: 3-methylcrontonyl-CoA carboxylase (MCC), pyruvate carboxylase (PC), acetyl-CoA c ... Read the Article | 1 | 4 | Activity MD/PA |
| Birth Asphyxia | Perinatal asphyxia is a lack of blood flow or gas exchange to or from the fetus in the period immediately before, during, or after the birth process. ... Read the Article | 1 | 6 | Activity DO |
| Birth Asphyxia | Perinatal asphyxia is a lack of blood flow or gas exchange to or from the fetus in the period immediately before, during, or after the birth process. ... Read the Article | 1 | 6 | Activity MD/PA |
| Birth Trauma | This activity reviews common birth-related injuries. The mechanism of injury, clinical features, and management of various birth-related traumatic eve ... Read the Article | 1 | 5 | Activity DO |
| Birth Trauma | This activity reviews common birth-related injuries. The mechanism of injury, clinical features, and management of various birth-related traumatic eve ... Read the Article | 1 | 5 | Activity MD/PA |
| Bladder Exstrophy | Bladder exstrophy is a rare congenital anomaly characterized by a spectrum of anomalies involving the ventral body wall, urinary tract, genitalia, bon ... Read the Article | 1 | 5 | Activity DO |
| Bladder Exstrophy | Bladder exstrophy is a rare congenital anomaly characterized by a spectrum of anomalies involving the ventral body wall, urinary tract, genitalia, bon ... Read the Article | 1 | 5 | Activity MD/PA |
| Bochdalek Hernia | Bochdalek hernia is a developmental defect in the posterolateral diaphragm, allowing herniation of abdominal contents into the thorax causing mechanic ... Read the Article | 1 | 5 | Activity DO |
| Bochdalek Hernia | Bochdalek hernia is a developmental defect in the posterolateral diaphragm, allowing herniation of abdominal contents into the thorax causing mechanic ... Read the Article | 1 | 5 | Activity MD/PA |
| Brachycephaly | Brachycephaly is an infant skull deformity characterized by a shortened anteroposterior skull length and a widened biparietal diameter. This condition ... Read the Article | 1 | 5 | Activity DO |
| Brachycephaly | Brachycephaly is an infant skull deformity characterized by a shortened anteroposterior skull length and a widened biparietal diameter. This condition ... Read the Article | 1 | 5 | Activity MD/PA |
| Breast Milk Jaundice | Breast milk jaundice is a type of jaundice that occurs in neonates due to breastfeeding. It happens within the first week of life due to the abnormal ... Read the Article | 1.25 | 12 | Activity DO |
| Breast Milk Jaundice | Breast milk jaundice is a type of jaundice that occurs in neonates due to breastfeeding. It happens within the first week of life due to the abnormal ... Read the Article | 1.25 | 12 | Activity MD/PA |
| Brief Resolved Unexplained Event | In 2016, the American Academy of Pediatrics recommended replacing the term apparent life-threatening event (ALTE) with brief resolved unexplained even ... Read the Article | 1 | 6 | Activity DO |
| Brief Resolved Unexplained Event | In 2016, the American Academy of Pediatrics recommended replacing the term apparent life-threatening event (ALTE) with brief resolved unexplained even ... Read the Article | 1 | 6 | Activity MD/PA |
| Bronchial Atresia | Congenital bronchial atresia is a rare condition characterized by focal obliteration of a proximal segment of a bronchus. The apicoposterior segmental ... Read the Article | 1 | 5 | Activity DO |
| Bronchial Atresia | Congenital bronchial atresia is a rare condition characterized by focal obliteration of a proximal segment of a bronchus. The apicoposterior segmental ... Read the Article | 1 | 5 | Activity MD/PA |
| Bronchogenic Cyst | Bronchogenic cysts are foregut-derived cystic malformations of the respiratory tract. They are usually located within the mediastinum at an early stag ... Read the Article | 1 | 6 | Activity DO |
| Bronchogenic Cyst | Bronchogenic cysts are foregut-derived cystic malformations of the respiratory tract. They are usually located within the mediastinum at an early stag ... Read the Article | 1 | 6 | Activity MD/PA |
| Bronchopulmonary Dysplasia | Bronchopulmonary dysplasia is one of the most common causes of morbidity and mortality in preterm infants. Despite significant advances in preterm inf ... Read the Article | 1 | 6 | Activity DO |
| Bronchopulmonary Dysplasia | Bronchopulmonary dysplasia is one of the most common causes of morbidity and mortality in preterm infants. Despite significant advances in preterm inf ... Read the Article | 1 | 6 | Activity MD/PA |
| C 17 Hydroxylase Deficiency | Congenital adrenal hyperplasia (CAH) covers a group of autosomal recessive disorders caused by a deficiency of one of the enzymes required for the ste ... Read the Article | 1 | 6 | Activity DO |
| C 17 Hydroxylase Deficiency | Congenital adrenal hyperplasia (CAH) covers a group of autosomal recessive disorders caused by a deficiency of one of the enzymes required for the ste ... Read the Article | 1 | 6 | Activity MD/PA |
| Cafe Au Lait Macules | Cafe-au-lait macules (CALMs) are common pigmented lesions found in the general population. They can be described as well-circumscribed, pigmented macu ... Read the Article | 1.25 | 8 | Activity DO |
| Cafe Au Lait Macules | Cafe-au-lait macules (CALMs) are common pigmented lesions found in the general population. They can be described as well-circumscribed, pigmented macu ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Caput Succedaneum | Caput succedaneum is a condition in which edema is observed on an infant's scalp shortly after delivery. It is a benign condition associated with birt ... Read the Article | 1 | 7 | Activity DO |
| Caput Succedaneum | Caput succedaneum is a condition in which edema is observed on an infant's scalp shortly after delivery. It is a benign condition associated with birt ... Read the Article | 1 | 7 | Activity MD/PA |
| Cardiac Rhabdomyoma | Cardiac rhabdomyoma is a rare tumor. It arises from the striated muscles. It is a type of hamartoma seen in the pediatric age group. Although mostly a ... Read the Article | 1 | 6 | Activity DO |
| Cardiac Rhabdomyoma | Cardiac rhabdomyoma is a rare tumor. It arises from the striated muscles. It is a type of hamartoma seen in the pediatric age group. Although mostly a ... Read the Article | 1 | 6 | Activity MD/PA |
| Carnitine Deficiency | Carnitine deficiency is a condition characterized by low carnitine levels in the body. Carnitine deficiency could be primary (due to defect in carniti ... Read the Article | 1 | 5 | Activity DO |
| Carnitine Deficiency | Carnitine deficiency is a condition characterized by low carnitine levels in the body. Carnitine deficiency could be primary (due to defect in carniti ... Read the Article | 1 | 5 | Activity MD/PA |
| Cataract | A cataract is a disease of the eye in which the normally clear lens has opacified which obscures the passage of light. It is a gradually progressive d ... Read the Article | 1.25 | 12 | Activity DO |
| Cataract | A cataract is a disease of the eye in which the normally clear lens has opacified which obscures the passage of light. It is a gradually progressive d ... Read the Article | 1.25 | 12 | Activity MD/PA |
| Cataract Surgery | Cataracts are the world’s leading cause of remediable blindness. While some cataracts, may be congenital, secondary to trauma, or drug-induced, most c ... Read the Article | 1.25 | 11 | Activity DO |
| Cataract Surgery | Cataracts are the world’s leading cause of remediable blindness. While some cataracts, may be congenital, secondary to trauma, or drug-induced, most c ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Catheter Management Of Ventricular Septal Defect | Traditionally, ventricular septal defects (VSDs) have been closed with an open approach, but since then, a percutaneous transcatheter closure has been ... Read the Article | 1 | 6 | Activity DO |
| Catheter Management Of Ventricular Septal Defect | Traditionally, ventricular septal defects (VSDs) have been closed with an open approach, but since then, a percutaneous transcatheter closure has been ... Read the Article | 1 | 6 | Activity MD/PA |
| Cavum Septum Pellucidum | The septum pellucidum (meaning translucent wall in Latin - SP), also known as the ventricle of Sylvius, is a thin, triangular double membrane separati ... Read the Article | 1 | 6 | Activity DO |
| Cavum Septum Pellucidum | The septum pellucidum (meaning translucent wall in Latin - SP), also known as the ventricle of Sylvius, is a thin, triangular double membrane separati ... Read the Article | 1 | 6 | Activity MD/PA |
| Cavum Veli Interpositi | The velum interpositum (VI) is a membrane resulting from the superposition of two layers of the tela choroidea of the third ventricle demarcating a po ... Read the Article | 1 | 4 | Activity DO |
| Cavum Veli Interpositi | The velum interpositum (VI) is a membrane resulting from the superposition of two layers of the tela choroidea of the third ventricle demarcating a po ... Read the Article | 1 | 4 | Activity MD/PA |
| Central and Peripheral Cyanosis | Peripheral cyanosis is the bluish discoloration of the distal extremities (Hands, fingertips, toes), and can sometimes involve circumoral and periorbi ... Read the Article | 1 | 6 | Activity DO |
| Central and Peripheral Cyanosis | Peripheral cyanosis is the bluish discoloration of the distal extremities (Hands, fingertips, toes), and can sometimes involve circumoral and periorbi ... Read the Article | 1 | 6 | Activity MD/PA |
| Cephalohematoma | A cephalohematoma is an accumulation of blood under the scalp. During the birth process, small blood vessels on the head of the fetus are broken as a ... Read the Article | 1.25 | 9 | Activity DO |
| Cephalohematoma | A cephalohematoma is an accumulation of blood under the scalp. During the birth process, small blood vessels on the head of the fetus are broken as a ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Cerebral Palsy | Cerebral palsy is a group of permanent disorders affecting the development of movement and causing a limitation of activity. Non-progressive disturban ... Read the Article | 1.25 | 11 | Activity DO |
| Cerebral Palsy | Cerebral palsy is a group of permanent disorders affecting the development of movement and causing a limitation of activity. Non-progressive disturban ... Read the Article | 1.25 | 11 | Activity MD/PA |
| CHARGE Syndrome | CHARGE syndrome is an inherited disorder caused by a mutation in the DNA-binding protein-7 CHD7 gene. CHARGE syndrome is an acronym for coloboma, hear ... Read the Article | 1 | 6 | Activity DO |
| CHARGE Syndrome | CHARGE syndrome is an inherited disorder caused by a mutation in the DNA-binding protein-7 CHD7 gene. CHARGE syndrome is an acronym for coloboma, hear ... Read the Article | 1 | 6 | Activity MD/PA |
| Chest Wall Deformities | Chest wall deformities are a set of congenital diseases; these can manifest as; an isolated feature, with other congenital anomalies, or as part of a ... Read the Article | 1.25 | 9 | Activity DO |
| Chest Wall Deformities | Chest wall deformities are a set of congenital diseases; these can manifest as; an isolated feature, with other congenital anomalies, or as part of a ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Chiari II Malformation | Chiari II malformation is a relatively common congenital malformation of the posterior fossa and the spine characterized by beaked midbrain, downward ... Read the Article | 1 | 6 | Activity DO |
| Chiari II Malformation | Chiari II malformation is a relatively common congenital malformation of the posterior fossa and the spine characterized by beaked midbrain, downward ... Read the Article | 1 | 6 | Activity MD/PA |
| Child Development | The stages through which a child goes through from birth until he or she becomes an adult is child development. Children are first newborns, and durin ... Read the Article | 4.5 | 85 | Activity DO |
| Child Development | The stages through which a child goes through from birth until he or she becomes an adult is child development. Children are first newborns, and durin ... Read the Article | 4.5 | 85 | Activity MD/PA |
| Child Intussusception | Intussusception is a condition in which part of the intestine folds into the section next to it. Intussusception usually involves the small bowel and ... Read the Article | 1.25 | 12 | Activity DO |
| Child Intussusception | Intussusception is a condition in which part of the intestine folds into the section next to it. Intussusception usually involves the small bowel and ... Read the Article | 1.25 | 12 | Activity MD/PA |
| Chlamydia | Chlamydia trachomatis is responsible for the greatest number of sexually transmitted infections and the majority of infection-related of blindness wor ... Read the Article | 1.5 | 13 | Activity DO |
| Chlamydia | Chlamydia trachomatis is responsible for the greatest number of sexually transmitted infections and the majority of infection-related of blindness wor ... Read the Article | 1.5 | 13 | Activity MD/PA |
| Chlamydia Pneumonia | Three species of Chlamydia namely, C. pneumoniae, C. psittaci, and C. trachomatis are known to cause respiratory infections in humans. They are one of ... Read the Article | 1.25 | 9 | Activity DO |
| Chlamydia Pneumonia | Three species of Chlamydia namely, C. pneumoniae, C. psittaci, and C. trachomatis are known to cause respiratory infections in humans. They are one of ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Choanal Atresia | The nasal choanae are paired openings that connect the nasal cavity with the nasopharynx. Choanal atresia is a congenital condition in which these ope ... Read the Article | 1 | 6 | Activity DO |
| Choanal Atresia | The nasal choanae are paired openings that connect the nasal cavity with the nasopharynx. Choanal atresia is a congenital condition in which these ope ... Read the Article | 1 | 6 | Activity MD/PA |
| Choledochal Cyst | A choledochal cyst (CC) or biliary cyst is a congenital or acquired anomaly affecting the biliary tree. It involves the dilation of the biliary tree t ... Read the Article | 1.5 | 14 | Activity DO |
| Choledochal Cyst | A choledochal cyst (CC) or biliary cyst is a congenital or acquired anomaly affecting the biliary tree. It involves the dilation of the biliary tree t ... Read the Article | 1.5 | 14 | Activity MD/PA |
| Chorioamnionitis | Chorioamnionitis is an infection that can occur before labor, during labor, or after delivery. It can be acute, subacute, or chronic. Chorioamnionitis ... Read the Article | 1 | 6 | Activity DO |
| Chorioamnionitis | Chorioamnionitis is an infection that can occur before labor, during labor, or after delivery. It can be acute, subacute, or chronic. Chorioamnionitis ... Read the Article | 1 | 6 | Activity MD/PA |
| Chorioretinitis | Chorioretinitis is a type of uveitis affecting the posterior segment of the eye. It is a vision-threatening condition that is associated with many sys ... Read the Article | 1 | 6 | Activity DO |
| Chorioretinitis | Chorioretinitis is a type of uveitis affecting the posterior segment of the eye. It is a vision-threatening condition that is associated with many sys ... Read the Article | 1 | 6 | Activity MD/PA |
| Choroid Plexus Papilloma | Choroid plexus papillomas (CPPs) are rare central nervous system tumors. They may be seen at any age, but are more common in infants. Their site of oc ... Read the Article | 1 | 4 | Activity DO |
| Choroid Plexus Papilloma | Choroid plexus papillomas (CPPs) are rare central nervous system tumors. They may be seen at any age, but are more common in infants. Their site of oc ... Read the Article | 1 | 4 | Activity MD/PA |
| Chronic Granulomatous Disease | Chronic granulomatous diseases (CGD) are a group of recurrent life-threatening infections due to a hereditary defect in forming reactive oxygen specie ... Read the Article | 1.5 | 16 | Activity DO |
| Chronic Granulomatous Disease | Chronic granulomatous diseases (CGD) are a group of recurrent life-threatening infections due to a hereditary defect in forming reactive oxygen specie ... Read the Article | 1.5 | 16 | Activity MD/PA |
| Cleft Hand | Cleft hand, otherwise referred to as ectrodactyly or colloquially as "split hand," is defined as a central longitudinal deficiency expressed as suppre ... Read the Article | 1 | 5 | Activity DO |
| Cleft Hand | Cleft hand, otherwise referred to as ectrodactyly or colloquially as "split hand," is defined as a central longitudinal deficiency expressed as suppre ... Read the Article | 1 | 5 | Activity MD/PA |
| Cleft Lip | Cleft lip deformity is one of the most common congenital deformities, and management requires an interprofessional approach to address the physical cl ... Read the Article | 1.25 | 9 | Activity DO |
| Cleft Lip | Cleft lip deformity is one of the most common congenital deformities, and management requires an interprofessional approach to address the physical cl ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Cleft Palate | Cleft palate is a developmental defect in the hard palate that results in a communication between the oral and nasal cavities resulting in nasal reflu ... Read the Article | 1.25 | 10 | Activity DO |
| Cleft Palate | Cleft palate is a developmental defect in the hard palate that results in a communication between the oral and nasal cavities resulting in nasal reflu ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Cloacal Malformations | Cloacal malformations are rare congenital anomalies characterized by a confluence of the gastrointestinal, genital, and urologic systems which exits t ... Read the Article | 1 | 3 | Activity DO |
| Cloacal Malformations | Cloacal malformations are rare congenital anomalies characterized by a confluence of the gastrointestinal, genital, and urologic systems which exits t ... Read the Article | 1 | 3 | Activity MD/PA |
| Clubfoot | Clubfoot is a congenital deformity of the foot, otherwise known as congenital talipes equinovarus. It is one of the most common congenital malformatio ... Read the Article | 1.25 | 9 | Activity DO |
| Clubfoot | Clubfoot is a congenital deformity of the foot, otherwise known as congenital talipes equinovarus. It is one of the most common congenital malformatio ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Coarctation of the Aorta | Coarctation of the aorta is a narrowing of the aorta, most commonly occurring just beyond the left subclavian artery. However, it can occur in various ... Read the Article | 1.5 | 14 | Activity DO |
| Coarctation of the Aorta | Coarctation of the aorta is a narrowing of the aorta, most commonly occurring just beyond the left subclavian artery. However, it can occur in various ... Read the Article | 1.5 | 14 | Activity MD/PA |
| Cockayne Syndrome | Cockayne syndrome, first described in 1936 by Dr. Cockayne, is a rare genetic disorder, mainly characterized by growth disorders, intellectual deficit ... Read the Article | 1 | 4 | Activity DO |
| Cockayne Syndrome | Cockayne syndrome, first described in 1936 by Dr. Cockayne, is a rare genetic disorder, mainly characterized by growth disorders, intellectual deficit ... Read the Article | 1 | 4 | Activity MD/PA |
| Colic | Infant colic is estimated to affect 20% of all infants. Despite its prevalence, a clear cause for infantile colic remains elusive. There have been man ... Read the Article | 1 | 5 | Activity DO |
| Colic | Infant colic is estimated to affect 20% of all infants. Despite its prevalence, a clear cause for infantile colic remains elusive. There have been man ... Read the Article | 1 | 5 | Activity MD/PA |
| Congenital Adrenal Hyperplasia | Congenital adrenal hyperplasia (CAH) is an autosomal recessive disease emerging from mutations of genes for enzymes that lead to the production of glu ... Read the Article | 1.25 | 10 | Activity DO |
| Congenital Adrenal Hyperplasia | Congenital adrenal hyperplasia (CAH) is an autosomal recessive disease emerging from mutations of genes for enzymes that lead to the production of glu ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Congenital Cytomegalovirus Infection | Primary cytomegalovirus (CMV) infection in pregnancy is associated with the highest risk of trans-placental transmission. Universal screening for pre ... Read the Article | 1.25 | 8 | Activity DO |
| Congenital Cytomegalovirus Infection | Primary cytomegalovirus (CMV) infection in pregnancy is associated with the highest risk of trans-placental transmission. Universal screening for pre ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Congenital Diaphragmatic Hernia | Congenital diaphragmatic hernia is a condition resulting from the herniation of abdominal contents into the thoracic cavity resulting in lung hypoplas ... Read the Article | 1.5 | 14 | Activity DO |
| Congenital Diaphragmatic Hernia | Congenital diaphragmatic hernia is a condition resulting from the herniation of abdominal contents into the thoracic cavity resulting in lung hypoplas ... Read the Article | 1.5 | 14 | Activity MD/PA |
| Congenital Herpes Simplex | Herpes simplex virus (HSV) infection in newborn infants can show up as the following: Disseminated disease involving multiple organs, most prominentl ... Read the Article | 1 | 5 | Activity DO |
| Congenital Herpes Simplex | Herpes simplex virus (HSV) infection in newborn infants can show up as the following: Disseminated disease involving multiple organs, most prominentl ... Read the Article | 1 | 5 | Activity MD/PA |
| Congenital Hypothyroidism | Congenital hypothyroidism is one of the most common preventable causes of intellectual disability. This activity reviews the evaluation and treatment ... Read the Article | 1.25 | 9 | Activity DO |
| Congenital Hypothyroidism | Congenital hypothyroidism is one of the most common preventable causes of intellectual disability. This activity reviews the evaluation and treatment ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Congenital Lobar Emphysema | Congenital lobar emphysema is a rare developmental anomaly of lungs that occurs mostly due to defective bronchial cartilages. It is diagnosed with a c ... Read the Article | 1.25 | 9 | Activity DO |
| Congenital Lobar Emphysema | Congenital lobar emphysema is a rare developmental anomaly of lungs that occurs mostly due to defective bronchial cartilages. It is diagnosed with a c ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Congenital Melanocytic Nevi | Congenital melanocytic nevi are benign skin lesions that usually present at birth and vary from small to large in size. Larger lesions are rarer and h ... Read the Article | 1 | 5 | Activity DO |
| Congenital Melanocytic Nevi | Congenital melanocytic nevi are benign skin lesions that usually present at birth and vary from small to large in size. Larger lesions are rarer and h ... Read the Article | 1 | 5 | Activity MD/PA |
| Congenital Myotonic Dystrophy | Congenital myotonic dystrophy (CMD) is an autosomal dominant neuromuscular disorder with multisystem involvement. It is a subtype of myotonic dystroph ... Read the Article | 1.25 | 10 | Activity DO |
| Congenital Myotonic Dystrophy | Congenital myotonic dystrophy (CMD) is an autosomal dominant neuromuscular disorder with multisystem involvement. It is a subtype of myotonic dystroph ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Congenital Nephrotic Syndrome | Congenital nephrotic syndrome (CNS) is defined when it presents within three months of birth. It consists of heavy proteinuria, edema, hypoalbuminemia ... Read the Article | 1 | 5 | Activity DO |
| Congenital Nephrotic Syndrome | Congenital nephrotic syndrome (CNS) is defined when it presents within three months of birth. It consists of heavy proteinuria, edema, hypoalbuminemia ... Read the Article | 1 | 5 | Activity MD/PA |
| Congenital Nevus | Congenital melanocytic nevi are pigmented lesions that are usually present a birth. They are generally benign, but a small percentage (especially the ... Read the Article | 1.25 | 11 | Activity DO |
| Congenital Nevus | Congenital melanocytic nevi are pigmented lesions that are usually present a birth. They are generally benign, but a small percentage (especially the ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Congenital Pulmonary Airway Malformation | Congenital pulmonary airway malformation is a congenital lung disease that can present from the prenatal period to childhood. Though rare overall, it ... Read the Article | 1 | 6 | Activity DO |
| Congenital Pulmonary Airway Malformation | Congenital pulmonary airway malformation is a congenital lung disease that can present from the prenatal period to childhood. Though rare overall, it ... Read the Article | 1 | 6 | Activity MD/PA |
| Congenital Rubella | Rubella, also known as German Measles, is a viral illness characterized by maculopapular rash, lymphadenopathy, and fever. It is a highly contagious b ... Read the Article | 1.25 | 10 | Activity DO |
| Congenital Rubella | Rubella, also known as German Measles, is a viral illness characterized by maculopapular rash, lymphadenopathy, and fever. It is a highly contagious b ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Congenital Syphilis | Congenital syphilis (CS) is caused by transmission of the spirochete Treponema pallidum from mother to fetus, resulting in diverse clinical presentati ... Read the Article | 1 | 7 | Activity DO |
| Congenital Syphilis | Congenital syphilis (CS) is caused by transmission of the spirochete Treponema pallidum from mother to fetus, resulting in diverse clinical presentati ... Read the Article | 1 | 7 | Activity MD/PA |
| Congenital Torticollis | Torticollis, also known as a twisted neck, is the contraction or contracture of the muscles of the neck that causes the head to tilt to one side. It i ... Read the Article | 1 | 5 | Activity DO |
| Congenital Torticollis | Torticollis, also known as a twisted neck, is the contraction or contracture of the muscles of the neck that causes the head to tilt to one side. It i ... Read the Article | 1 | 5 | Activity MD/PA |
| Congenital Toxoplasmosis | Toxoplasmosis is a parasitic infection in humans and animals. Infection in healthy immunocompetent adults is asymptomatic in about 50% of the cases al ... Read the Article | 1.25 | 8 | Activity DO |
| Congenital Toxoplasmosis | Toxoplasmosis is a parasitic infection in humans and animals. Infection in healthy immunocompetent adults is asymptomatic in about 50% of the cases al ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Congenital Unilateral Lower Lip Palsy | Congenital unilateral lower lip palsy is a congenital anomaly that is caused by agenesis or hypoplasia of depressor anguli oris muscle. Unilateral dep ... Read the Article | 1 | 5 | Activity DO |
| Congenital Unilateral Lower Lip Palsy | Congenital unilateral lower lip palsy is a congenital anomaly that is caused by agenesis or hypoplasia of depressor anguli oris muscle. Unilateral dep ... Read the Article | 1 | 5 | Activity MD/PA |
| Congenital Varicella Syndrome | The varicella-zoster virus (VZV) is a highly contagious virus of the herpes family. Chickenpox (or primary VZV infection) is a common childhood diseas ... Read the Article | 1 | 6 | Activity DO |
| Congenital Varicella Syndrome | The varicella-zoster virus (VZV) is a highly contagious virus of the herpes family. Chickenpox (or primary VZV infection) is a common childhood diseas ... Read the Article | 1 | 6 | Activity MD/PA |
| Conjoined Twins | Conjoined twins refers to twins that are physically fused in utero and consequently at birth. This type of pregnancy is a complicated phenomenon that ... Read the Article | 1 | 4 | Activity DO |
| Conjoined Twins | Conjoined twins refers to twins that are physically fused in utero and consequently at birth. This type of pregnancy is a complicated phenomenon that ... Read the Article | 1 | 4 | Activity MD/PA |
| Cornelia de Lange Syndrome | Cornelia de Lange syndrome (CdLS) was initially described in 1933. CdLS is a genetic disorder that affects many organs, leading to various clinical pr ... Read the Article | 1 | 6 | Activity DO |
| Cornelia de Lange Syndrome | Cornelia de Lange syndrome (CdLS) was initially described in 1933. CdLS is a genetic disorder that affects many organs, leading to various clinical pr ... Read the Article | 1 | 6 | Activity MD/PA |
| Coronary Cameral Fistula | Coronary cameral fistula is an abnormal communication existing between a coronary artery and any cardiac chamber. It appears in less than 1% of the po ... Read the Article | 1 | 5 | Activity DO |
| Coronary Cameral Fistula | Coronary cameral fistula is an abnormal communication existing between a coronary artery and any cardiac chamber. It appears in less than 1% of the po ... Read the Article | 1 | 5 | Activity MD/PA |
| Cradle Cap | Cradle cap, or pityriasis capitis, is a subset of infantile seborrheic dermatitis (ISD). It is a very common, mostly self-limiting, chronic non-inflam ... Read the Article | 1 | 5 | Activity DO |
| Cradle Cap | Cradle cap, or pityriasis capitis, is a subset of infantile seborrheic dermatitis (ISD). It is a very common, mostly self-limiting, chronic non-inflam ... Read the Article | 1 | 5 | Activity MD/PA |
| Craniosynostosis | Craniosynostosis results from the premature closure of one or more sutures of the skull. Depending on the number of sutures involved, and the range of ... Read the Article | 1 | 7 | Activity DO |
| Craniosynostosis | Craniosynostosis results from the premature closure of one or more sutures of the skull. Depending on the number of sutures involved, and the range of ... Read the Article | 1 | 7 | Activity MD/PA |
| Cri Du Chat Syndrome | Cri du chat syndrome is a genetic disorder caused by a deletion of the short arm of chromosome 5. The name of the syndrome means the cry of the cat an ... Read the Article | 1 | 5 | Activity DO |
| Cri Du Chat Syndrome | Cri du chat syndrome is a genetic disorder caused by a deletion of the short arm of chromosome 5. The name of the syndrome means the cry of the cat an ... Read the Article | 1 | 5 | Activity MD/PA |
| Crigler Najjar Syndrome | Crigler-Najjar syndrome is an autosomal recessive inherited disorder that leads to congenital non-hemolytic jaundice. Crigler-Najjar syndrome is cause ... Read the Article | 1 | 5 | Activity DO |
| Crigler Najjar Syndrome | Crigler-Najjar syndrome is an autosomal recessive inherited disorder that leads to congenital non-hemolytic jaundice. Crigler-Najjar syndrome is cause ... Read the Article | 1 | 5 | Activity MD/PA |
| Cryptorchidism | Cryptorchidism is the absence of at least one testicle from the scrotum. It is the most common birth defect involving the male genitalia. About 3% of ... Read the Article | 1.5 | 14 | Activity DO |
| Cryptorchidism | Cryptorchidism is the absence of at least one testicle from the scrotum. It is the most common birth defect involving the male genitalia. About 3% of ... Read the Article | 1.5 | 14 | Activity MD/PA |
| Cultural Competence in the Care of Muslim Patients and Their Families | Delivering high-quality care to patients of the Muslim faith requires knowledge of the differences in cultural and spiritual values. Important differe ... Read the Article | 1.5 | 17 | Activity DO |
| Cultural Competence in the Care of Muslim Patients and Their Families | Delivering high-quality care to patients of the Muslim faith requires knowledge of the differences in cultural and spiritual values. Important differe ... Read the Article | 1.5 | 17 | Activity MD/PA |
| Cutis Marmorata Telangiectatica Congenita | Cutis marmorata telangiectatica (CMTC) is a rare, sporadic, congenital cutaneous vascular disorder of unknown etiology. CMTC usually presents at birth ... Read the Article | 1 | 6 | Activity DO |
| Cutis Marmorata Telangiectatica Congenita | Cutis marmorata telangiectatica (CMTC) is a rare, sporadic, congenital cutaneous vascular disorder of unknown etiology. CMTC usually presents at birth ... Read the Article | 1 | 6 | Activity MD/PA |
| Cyanosis | Cyanosis is characterized by a blueish discoloration of the skin or mucous membranes. Cyanosis is frequently encountered in clinical practice, and the ... Read the Article | 1 | 4 | Activity DO |
| Cyanosis | Cyanosis is characterized by a blueish discoloration of the skin or mucous membranes. Cyanosis is frequently encountered in clinical practice, and the ... Read the Article | 1 | 4 | Activity MD/PA |
| Cyanotic Heart Disease | Congenital heart disease (CHD) are structural abnormalities of the heart or intrathoracic great vessels occurring during fetal development. CHD is the ... Read the Article | 1.25 | 8 | Activity DO |
| Cyanotic Heart Disease | Congenital heart disease (CHD) are structural abnormalities of the heart or intrathoracic great vessels occurring during fetal development. CHD is the ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Cystic Fibrosis | Until relatively modern times, cystic fibrosis was poorly understood. In 1949, Lowe et al. postulated that cystic fibrosis must be caused by a geneti ... Read the Article | 2.75 | 44 | Activity DO |
| Cystic Fibrosis | Until relatively modern times, cystic fibrosis was poorly understood. In 1949, Lowe et al. postulated that cystic fibrosis must be caused by a geneti ... Read the Article | 2.75 | 44 | Activity MD/PA |
| Cystic Hygroma | Cystic hygromas are the most common subtype of lymphangiomas, presenting at birth and in early infancy. Enlargement of cystic hygromas is common, and ... Read the Article | 1 | 7 | Activity DO |
| Cystic Hygroma | Cystic hygromas are the most common subtype of lymphangiomas, presenting at birth and in early infancy. Enlargement of cystic hygromas is common, and ... Read the Article | 1 | 7 | Activity MD/PA |
| Dacryocystitis | Dacryocystitis is characterized as an inflammatory state of the nasolacrimal sac. It is typically caused by an obstruction within the nasolacrimal duc ... Read the Article | 1 | 6 | Activity DO |
| Dacryocystitis | Dacryocystitis is characterized as an inflammatory state of the nasolacrimal sac. It is typically caused by an obstruction within the nasolacrimal duc ... Read the Article | 1 | 6 | Activity MD/PA |
| Dacryostenosis | Dacryostenosis is an acquired or congenital condition that can cause epiphora but can progress to dacryocystitis in children and in adults. This activ ... Read the Article | 1 | 5 | Activity DO |
| Dacryostenosis | Dacryostenosis is an acquired or congenital condition that can cause epiphora but can progress to dacryocystitis in children and in adults. This activ ... Read the Article | 1 | 5 | Activity MD/PA |
| Delayed Hypersensitivity Reactions | Coombs and Gel classified type IV hypersensitivity reaction (HR) as a delayed hypersensitivity reaction (DHR), which takes more than 12 hours to devel ... Read the Article | 1.25 | 8 | Activity DO |
| Delayed Hypersensitivity Reactions | Coombs and Gel classified type IV hypersensitivity reaction (HR) as a delayed hypersensitivity reaction (DHR), which takes more than 12 hours to devel ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Developmental Dysplasia Of The Hip | DDH (developmental dysplasia of the hip ) is a disorder that is due to abnormal development of acetabulum with or without hip dislocation. Early diagn ... Read the Article | 1.25 | 11 | Activity DO |
| Developmental Dysplasia Of The Hip | DDH (developmental dysplasia of the hip ) is a disorder that is due to abnormal development of acetabulum with or without hip dislocation. Early diagn ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Dextrocardia | Dextrocardia is a congenital condition in which the heart is located in the right side of the thorax. This activity reviews the evaluation and managem ... Read the Article | 1 | 5 | Activity DO |
| Dextrocardia | Dextrocardia is a congenital condition in which the heart is located in the right side of the thorax. This activity reviews the evaluation and managem ... Read the Article | 1 | 5 | Activity MD/PA |
| Diabetic Embryopathy | Maternal diabetes has several adverse effects on embryogenesis and fetal development and causes multiple congenital anomalies, and secondary medical c ... Read the Article | 1 | 6 | Activity DO |
| Diabetic Embryopathy | Maternal diabetes has several adverse effects on embryogenesis and fetal development and causes multiple congenital anomalies, and secondary medical c ... Read the Article | 1 | 6 | Activity MD/PA |
| Diamond Blackfan Anemia | Diamond Blackfan anemia (DBA) is a congenital type of anemia with pure red cell aplasia causing congenital bone abnormalities and most commonly presen ... Read the Article | 1 | 5 | Activity DO |
| Diamond Blackfan Anemia | Diamond Blackfan anemia (DBA) is a congenital type of anemia with pure red cell aplasia causing congenital bone abnormalities and most commonly presen ... Read the Article | 1 | 5 | Activity MD/PA |
| DiGeorge Syndrome | DiGeorge syndrome (DGS) is a congenital disorder with a broad phenotypic presentation, which results predominantly from the microdeletion of chromosom ... Read the Article | 1.25 | 7 | Activity DO |
| DiGeorge Syndrome | DiGeorge syndrome (DGS) is a congenital disorder with a broad phenotypic presentation, which results predominantly from the microdeletion of chromosom ... Read the Article | 1.25 | 7 | Activity MD/PA |
| Down Syndrome | Down syndrome (trisomy 21) is a genetic disorder caused by the presence of all or a portion of a third chromosome 21. Patients typically present with ... Read the Article | 1.5 | 16 | Activity DO |
| Down Syndrome | Down syndrome (trisomy 21) is a genetic disorder caused by the presence of all or a portion of a third chromosome 21. Patients typically present with ... Read the Article | 1.5 | 16 | Activity MD/PA |
| Duodenal Atresia And Stenosis | Duodenal atresia is a congenital intestinal obstruction that can cause bilious or non bilious vomiting within the first 24 to 38 hours of neonatal lif ... Read the Article | 1.25 | 12 | Activity DO |
| Duodenal Atresia And Stenosis | Duodenal atresia is a congenital intestinal obstruction that can cause bilious or non bilious vomiting within the first 24 to 38 hours of neonatal lif ... Read the Article | 1.25 | 12 | Activity MD/PA |
| Ebstein Anomaly And Malformation | Ebstein anomaly of the tricuspid valve is a congenital malformation, in which there is downward displacement of insertion of septal and posterior leaf ... Read the Article | 1 | 5 | Activity DO |
| Ebstein Anomaly And Malformation | Ebstein anomaly of the tricuspid valve is a congenital malformation, in which there is downward displacement of insertion of septal and posterior leaf ... Read the Article | 1 | 5 | Activity MD/PA |
| Echocardiogram | Cardiac echocardiography is a safe and non-invasive test that provides the clinical team with important cardiac function data. This functional data is ... Read the Article | 1.25 | 8 | Activity DO |
| Echocardiogram | Cardiac echocardiography is a safe and non-invasive test that provides the clinical team with important cardiac function data. This functional data is ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Ectodermal Dysplasia | Ectodermal dysplasias form a diverse group of inherited disorders characterized by a congenital defect in two or more ectodermal structures, one of wh ... Read the Article | 1 | 5 | Activity DO |
| Ectodermal Dysplasia | Ectodermal dysplasias form a diverse group of inherited disorders characterized by a congenital defect in two or more ectodermal structures, one of wh ... Read the Article | 1 | 5 | Activity MD/PA |
| Ectopic Pregnancy, Ultrasound | Ectopic pregnancy is a diagnosis that is quite challenging to make. It has been estimated that 40% of ectopic pregnancies go undiagnosed on initial pr ... Read the Article | 1 | 5 | Activity DO |
| Ectopic Pregnancy, Ultrasound | Ectopic pregnancy is a diagnosis that is quite challenging to make. It has been estimated that 40% of ectopic pregnancies go undiagnosed on initial pr ... Read the Article | 1 | 5 | Activity MD/PA |
| Edward Syndrome | Edward syndrome was first reported by Edwards et al. in 1960, who reported a neonate with multiple congenital malformations and cognitive deficit. Thi ... Read the Article | 1.25 | 9 | Activity DO |
| Edward Syndrome | Edward syndrome was first reported by Edwards et al. in 1960, who reported a neonate with multiple congenital malformations and cognitive deficit. Thi ... Read the Article | 1.25 | 9 | Activity MD/PA |
| EEG Neonatal Visual Analysis | An electroencephalogram (EEG) is a useful ancillary and diagnostic test that detects electrical activity in the brain. The neonatal EEG can be quite c ... Read the Article | 1 | 4 | Activity DO |
| EEG Neonatal Visual Analysis | An electroencephalogram (EEG) is a useful ancillary and diagnostic test that detects electrical activity in the brain. The neonatal EEG can be quite c ... Read the Article | 1 | 4 | Activity MD/PA |
| Ehlers Danlos Syndrome | Ehlers-Danlos syndrome (EDS) is a genetic disorder affecting collagen formation and function. It affects virtually every organ system, which can resul ... Read the Article | 1.25 | 9 | Activity DO |
| Ehlers Danlos Syndrome | Ehlers-Danlos syndrome (EDS) is a genetic disorder affecting collagen formation and function. It affects virtually every organ system, which can resul ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Encephalocele | Encephalocele is usually a congenital type of neural tube defect, where a sac containing brain/meninges/cerebrospinal fluid forms outside the skull du ... Read the Article | 1 | 5 | Activity DO |
| Encephalocele | Encephalocele is usually a congenital type of neural tube defect, where a sac containing brain/meninges/cerebrospinal fluid forms outside the skull du ... Read the Article | 1 | 5 | Activity MD/PA |
| Endotracheal Tube | In its simplest form, the endotracheal tube is a tube constructed of polyvinyl chloride that is placed between the vocal cords through the trachea. It ... Read the Article | 1.5 | 16 | Activity DO |
| Endotracheal Tube | In its simplest form, the endotracheal tube is a tube constructed of polyvinyl chloride that is placed between the vocal cords through the trachea. It ... Read the Article | 1.5 | 16 | Activity MD/PA |
| Epidermal Nevus Syndromes | Epidermal nevus syndrome is an umbrella term used to describe epidermal nevi in association with syndromic features. The first well-described syndrome ... Read the Article | 1 | 5 | Activity DO |
| Epidermal Nevus Syndromes | Epidermal nevus syndrome is an umbrella term used to describe epidermal nevi in association with syndromic features. The first well-described syndrome ... Read the Article | 1 | 5 | Activity MD/PA |
| Epidermolytic Hyperkeratosis | Epidermolytic hyperkeratosis (bullous ichthyosiform erythroderma) is a rare autosomal dominant disorder of cornification caused by mutations in kerati ... Read the Article | 1 | 5 | Activity DO |
| Epidermolytic Hyperkeratosis | Epidermolytic hyperkeratosis (bullous ichthyosiform erythroderma) is a rare autosomal dominant disorder of cornification caused by mutations in kerati ... Read the Article | 1 | 5 | Activity MD/PA |
| Epstein Pearls | Epstein pearls are small, benign, self-resolving nodules commonly found in the oral cavities of newborns. This activity describes the evaluation and m ... Read the Article | 1.25 | 10 | Activity DO |
| Epstein Pearls | Epstein pearls are small, benign, self-resolving nodules commonly found in the oral cavities of newborns. This activity describes the evaluation and m ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Erb Palsy | Erb palsy, or Erb-Duchenne paralysis, is one of the most common neurological birth injuries. It is caused by injury to the brachial plexus, which is f ... Read the Article | 1 | 5 | Activity DO |
| Erb Palsy | Erb palsy, or Erb-Duchenne paralysis, is one of the most common neurological birth injuries. It is caused by injury to the brachial plexus, which is f ... Read the Article | 1 | 5 | Activity MD/PA |
| Erythema Toxicum | Erythema toxicum neonatorum is a condition that has been described (rash) as early as the 15th century by a pediatrician named B. Metlinger. It has be ... Read the Article | 1 | 5 | Activity DO |
| Erythema Toxicum | Erythema toxicum neonatorum is a condition that has been described (rash) as early as the 15th century by a pediatrician named B. Metlinger. It has be ... Read the Article | 1 | 5 | Activity MD/PA |
| Erythroblastosis Fetalis | Hemolytic disease of the fetus and newborn (HDFN) is also known as alloimmune HDFN or erythroblastosis fetalis. It is caused by the destruction of neo ... Read the Article | 1.25 | 8 | Activity DO |
| Erythroblastosis Fetalis | Hemolytic disease of the fetus and newborn (HDFN) is also known as alloimmune HDFN or erythroblastosis fetalis. It is caused by the destruction of neo ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Erythropoietin | Erythropoietin (EPO) is a glycoprotein hormone, naturally produced by the peritubular cells of the kidney, that stimulates red blood cell production. ... Read the Article | 1 | 7 | Activity DO |
| Erythropoietin | Erythropoietin (EPO) is a glycoprotein hormone, naturally produced by the peritubular cells of the kidney, that stimulates red blood cell production. ... Read the Article | 1 | 7 | Activity MD/PA |
| Esophageal Atresia | The trachea and esophagus arise from a separation of a common foregut tube during early fetal development. Failure of separation or complete developme ... Read the Article | 1 | 6 | Activity DO |
| Esophageal Atresia | The trachea and esophagus arise from a separation of a common foregut tube during early fetal development. Failure of separation or complete developme ... Read the Article | 1 | 6 | Activity MD/PA |
| Exchange Transfusion | Therapeutic plasma exchange (TPE) is a procedure employed to "cleanse" the blood of various pathologic entities including antibodies, immune complexes ... Read the Article | 1 | 5 | Activity DO |
| Exchange Transfusion | Therapeutic plasma exchange (TPE) is a procedure employed to "cleanse" the blood of various pathologic entities including antibodies, immune complexes ... Read the Article | 1 | 5 | Activity MD/PA |
| External Cephalic Version | About 25 percent of fetuses will be in breech presentation at 28 weeks, though this decreases to roughly 3 to 4 percent at term. Most infants who are ... Read the Article | 1.25 | 8 | Activity DO |
| External Cephalic Version | About 25 percent of fetuses will be in breech presentation at 28 weeks, though this decreases to roughly 3 to 4 percent at term. Most infants who are ... Read the Article | 1.25 | 8 | Activity MD/PA |
| External Ear Aural Atresia | Aural atresia is the absence of a patent ear canal that may be acquired or congenital. To preserve hearing and allow normal speech and language develo ... Read the Article | 1 | 6 | Activity DO |
| External Ear Aural Atresia | Aural atresia is the absence of a patent ear canal that may be acquired or congenital. To preserve hearing and allow normal speech and language develo ... Read the Article | 1 | 6 | Activity MD/PA |
| Extracorporeal Membrane Oxygenation In Children | Extracorporeal membrane oxygenation (ECMO) is a well-known means of advanced life support in patients with significant cardiorespiratory impairment re ... Read the Article | 1 | 5 | Activity DO |
| Extracorporeal Membrane Oxygenation In Children | Extracorporeal membrane oxygenation (ECMO) is a well-known means of advanced life support in patients with significant cardiorespiratory impairment re ... Read the Article | 1 | 5 | Activity MD/PA |
| Eyelid Coloboma | Eyelid coloboma is a rare condition that affects congenitally. It’s a very annoying and disturbing condition for the parents also. While treating the ... Read the Article | 1 | 5 | Activity DO |
| Eyelid Coloboma | Eyelid coloboma is a rare condition that affects congenitally. It’s a very annoying and disturbing condition for the parents also. While treating the ... Read the Article | 1 | 5 | Activity MD/PA |
| Factor XIII Deficiency | Factor XIII deficiency is a rare bleeding disorder that is challenging to recognize clinically. The lab tests such as the prothrombin time, INR, and a ... Read the Article | 1 | 6 | Activity DO |
| Factor XIII Deficiency | Factor XIII deficiency is a rare bleeding disorder that is challenging to recognize clinically. The lab tests such as the prothrombin time, INR, and a ... Read the Article | 1 | 6 | Activity MD/PA |
| Fatty Liver In Pregnancy | Acute fatty liver in pregnancy (AFLP) is an obstetric emergency and carries high morbidity and mortality, including death in the mother and her fetus. ... Read the Article | 1 | 5 | Activity DO |
| Fatty Liver In Pregnancy | Acute fatty liver in pregnancy (AFLP) is an obstetric emergency and carries high morbidity and mortality, including death in the mother and her fetus. ... Read the Article | 1 | 5 | Activity MD/PA |
| Feeding Disability In Children | Feeding disability in children is an inadequacy of food intake that results in poor weight gain, failure to thrive, and/or delayed milestones. This ac ... Read the Article | 1 | 6 | Activity DO |
| Feeding Disability In Children | Feeding disability in children is an inadequacy of food intake that results in poor weight gain, failure to thrive, and/or delayed milestones. This ac ... Read the Article | 1 | 6 | Activity MD/PA |
| Fetal Growth Restriction | Fetal growth restriction (FGR) is most often defined as an estimated fetal weight less than the 10th percentile for gestational age by prenatal ultras ... Read the Article | 1.25 | 8 | Activity DO |
| Fetal Growth Restriction | Fetal growth restriction (FGR) is most often defined as an estimated fetal weight less than the 10th percentile for gestational age by prenatal ultras ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Fever In A Neonate | The World Health Organization categorizes neonatal sepsis as early or late based on the age of onset. Early neonatal sepsis affects infants less than ... Read the Article | 1 | 5 | Activity DO |
| Fever In A Neonate | The World Health Organization categorizes neonatal sepsis as early or late based on the age of onset. Early neonatal sepsis affects infants less than ... Read the Article | 1 | 5 | Activity MD/PA |
| Food Allergies | Food allergy is defined as an immune reaction to proteins in the food and can be immunoglobulin (Ig)E-mediated or non-IgE-mediated. IgE-mediated food ... Read the Article | 1.25 | 8 | Activity DO |
| Food Allergies | Food allergy is defined as an immune reaction to proteins in the food and can be immunoglobulin (Ig)E-mediated or non-IgE-mediated. IgE-mediated food ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Forceps Delivery | The use of forceps in infant delivery has fallen out of favor among obstetricians in the past three decades. Forceps deliveries now make up about only ... Read the Article | 1 | 7 | Activity DO |
| Forceps Delivery | The use of forceps in infant delivery has fallen out of favor among obstetricians in the past three decades. Forceps deliveries now make up about only ... Read the Article | 1 | 7 | Activity MD/PA |
| Fungal Endophthalmitis | Fungal endophthalmitis is a rare disease of ocular inflammation caused by fungal infections from either endogenous or exogenous sources. Because the c ... Read the Article | 1 | 5 | Activity DO |
| Fungal Endophthalmitis | Fungal endophthalmitis is a rare disease of ocular inflammation caused by fungal infections from either endogenous or exogenous sources. Because the c ... Read the Article | 1 | 5 | Activity MD/PA |
| Galactokinase Deficiency | Galactokinase deficiency or galactosemia type II is a rare inborn error of galactose metabolism. Galactosemia type II is rarer and more insidious than ... Read the Article | 1 | 4 | Activity DO |
| Galactokinase Deficiency | Galactokinase deficiency or galactosemia type II is a rare inborn error of galactose metabolism. Galactosemia type II is rarer and more insidious than ... Read the Article | 1 | 4 | Activity MD/PA |
| Galactose 1 Phosphate Uridyltransferase Deficiency | Galactosemia is an inborn error of metabolism due to impaired degradation of galactose. If not recognized and treated promptly, affected infants may d ... Read the Article | 1.25 | 13 | Activity DO |
| Galactose 1 Phosphate Uridyltransferase Deficiency | Galactosemia is an inborn error of metabolism due to impaired degradation of galactose. If not recognized and treated promptly, affected infants may d ... Read the Article | 1.25 | 13 | Activity MD/PA |
| Gastroschisis | Gastroschisis is a paraumbilical abdominal wall defect associated with protrusion of the bowel through the defect. A membrane does not cover the bowe ... Read the Article | 1.25 | 7 | Activity DO |
| Gastroschisis | Gastroschisis is a paraumbilical abdominal wall defect associated with protrusion of the bowel through the defect. A membrane does not cover the bowe ... Read the Article | 1.25 | 7 | Activity MD/PA |
| Glottic Stenosis | Glottic stenosis describes a narrowing of the portion of the larynx containing the vocal cords and glottic opening, otherwise known as the glottis. Gl ... Read the Article | 1 | 5 | Activity DO |
| Glottic Stenosis | Glottic stenosis describes a narrowing of the portion of the larynx containing the vocal cords and glottic opening, otherwise known as the glottis. Gl ... Read the Article | 1 | 5 | Activity MD/PA |
| Gonococcal Conjunctivitis | Gonococcal conjunctivitis (GC), also known as gonococcal ophthalmia neonatorum when it occurs in neonates, is an infection that is transmitted by cont ... Read the Article | 1 | 6 | Activity DO |
| Gonococcal Conjunctivitis | Gonococcal conjunctivitis (GC), also known as gonococcal ophthalmia neonatorum when it occurs in neonates, is an infection that is transmitted by cont ... Read the Article | 1 | 6 | Activity MD/PA |
| Gonorrhea | Neisseria gonorrhoeae, an obligate human pathogen, is a sexually transmitted disease that causes consequential worldwide morbidity both in resource-ab ... Read the Article | 1.75 | 21 | Activity DO |
| Gonorrhea | Neisseria gonorrhoeae, an obligate human pathogen, is a sexually transmitted disease that causes consequential worldwide morbidity both in resource-ab ... Read the Article | 1.75 | 21 | Activity MD/PA |
| Hemifacial Microsomia | Hemifacial microsomia is the second most common congenital craniofacial defect after cleft lip and palate. It can present with a spectrum of deformiti ... Read the Article | 1 | 5 | Activity DO |
| Hemifacial Microsomia | Hemifacial microsomia is the second most common congenital craniofacial defect after cleft lip and palate. It can present with a spectrum of deformiti ... Read the Article | 1 | 5 | Activity MD/PA |
| Hemolytic Diseases Of The Newborn | Hemolytic disease of the fetus and newborn is a red blood cell mismatch between mothers and their fetus that can cause significant morbidity and morta ... Read the Article | 1 | 6 | Activity DO |
| Hemolytic Diseases Of The Newborn | Hemolytic disease of the fetus and newborn is a red blood cell mismatch between mothers and their fetus that can cause significant morbidity and morta ... Read the Article | 1 | 6 | Activity MD/PA |
| Hemorrhagic Disease Of Newborn | Hemorrhagic disease of the newborn is a life-threatening condition that is due to insufficient vitamin K levels in newborns as a result of various cau ... Read the Article | 1.25 | 8 | Activity DO |
| Hemorrhagic Disease Of Newborn | Hemorrhagic disease of the newborn is a life-threatening condition that is due to insufficient vitamin K levels in newborns as a result of various cau ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Hepatic Hemangioma | Hemangiomas are benign vascular tumors that may involve either the skin or viscera. Infantile hemangioma (IH) grows rapidly after birth then involutes ... Read the Article | 1 | 7 | Activity DO |
| Hepatic Hemangioma | Hemangiomas are benign vascular tumors that may involve either the skin or viscera. Infantile hemangioma (IH) grows rapidly after birth then involutes ... Read the Article | 1 | 7 | Activity MD/PA |
| Hepatitis B | Hepatitis B infection is a serious global healthcare problem. Often transmitted via body fluids like blood, semen, and vaginal secretions, the hepatit ... Read the Article | 2 | 25 | Activity DO |
| Hepatitis B | Hepatitis B infection is a serious global healthcare problem. Often transmitted via body fluids like blood, semen, and vaginal secretions, the hepatit ... Read the Article | 2 | 25 | Activity MD/PA |
| Hepatitis B Vaccine | The hepatitis B vaccine is a medication used in the prevention of hepatitis B infection, which can lead to chronic liver failure and hepatocellular ca ... Read the Article | 1.5 | 16 | Activity DO |
| Hepatitis B Vaccine | The hepatitis B vaccine is a medication used in the prevention of hepatitis B infection, which can lead to chronic liver failure and hepatocellular ca ... Read the Article | 1.5 | 16 | Activity MD/PA |
| Hepatobiliary Iminodiacetic Acid Scan | Hepatobiliary scintigraphy is a diagnostic nuclear medicine procedure that uses radiotracers to evaluate the biliary system and indirectly, the liver. ... Read the Article | 1 | 6 | Activity DO |
| Hepatobiliary Iminodiacetic Acid Scan | Hepatobiliary scintigraphy is a diagnostic nuclear medicine procedure that uses radiotracers to evaluate the biliary system and indirectly, the liver. ... Read the Article | 1 | 6 | Activity MD/PA |
| Hereditary Elliptocytosis | Hereditary elliptocytosis is a group of inherited heterogenous red blood cell (RBC) membrane disorders characterized by elliptical-shaped RBCs. The pr ... Read the Article | 1 | 5 | Activity DO |
| Hereditary Elliptocytosis | Hereditary elliptocytosis is a group of inherited heterogenous red blood cell (RBC) membrane disorders characterized by elliptical-shaped RBCs. The pr ... Read the Article | 1 | 5 | Activity MD/PA |
| Hereditary Spherocytosis | Hereditary spherocytosis, a type of congenital hemolytic anemia, is the most prevalent cause of hemolytic anemia due to an abnormal red cell membrane. ... Read the Article | 1.75 | 20 | Activity DO |
| Hereditary Spherocytosis | Hereditary spherocytosis, a type of congenital hemolytic anemia, is the most prevalent cause of hemolytic anemia due to an abnormal red cell membrane. ... Read the Article | 1.75 | 20 | Activity MD/PA |
| Herpes Simplex Encephalitis | Herpes simplex encephalitis is caused by Herpes Simplex Virus type 1(HSV-1) or type 2 (HSV-2). HSV-1 causes encephalitis in children beyond the neonat ... Read the Article | 1.75 | 18 | Activity DO |
| Herpes Simplex Encephalitis | Herpes simplex encephalitis is caused by Herpes Simplex Virus type 1(HSV-1) or type 2 (HSV-2). HSV-1 causes encephalitis in children beyond the neonat ... Read the Article | 1.75 | 18 | Activity MD/PA |
| Herpes Simplex Neonatorum | Herpes simplex virus (HSV) infections in the neonatal period continue to be troublesome for practitioners. In the 1970s, the drug vidarabine was intro ... Read the Article | 1 | 4 | Activity DO |
| Herpes Simplex Neonatorum | Herpes simplex virus (HSV) infections in the neonatal period continue to be troublesome for practitioners. In the 1970s, the drug vidarabine was intro ... Read the Article | 1 | 4 | Activity MD/PA |
| High Frequency Ventilation | High-frequency ventilation (HFV) is a type of ventilation that is utilized when conventional ventilation fails. It is a technique where the set respir ... Read the Article | 1 | 6 | Activity DO |
| High Frequency Ventilation | High-frequency ventilation (HFV) is a type of ventilation that is utilized when conventional ventilation fails. It is a technique where the set respir ... Read the Article | 1 | 6 | Activity MD/PA |
| Hirschsprung Disease | Hirschsprung disease (HD) is a congenital disorder characterized by the absence of ganglion cells (GC) at the Meissner's plexus (submucosa) and Auerba ... Read the Article | 1.25 | 9 | Activity DO |
| Hirschsprung Disease | Hirschsprung disease (HD) is a congenital disorder characterized by the absence of ganglion cells (GC) at the Meissner's plexus (submucosa) and Auerba ... Read the Article | 1.25 | 9 | Activity MD/PA |
| HIV In Pregnancy | Several thousand HIV positive pregnant women give birth in the US annually. With proper management, these women can achieve viral suppression to undet ... Read the Article | 1.25 | 8 | Activity DO |
| HIV In Pregnancy | Several thousand HIV positive pregnant women give birth in the US annually. With proper management, these women can achieve viral suppression to undet ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Holoprosencephaly | Holoprosencephaly occurs as a result of anomalous signaling interactions between the neural crest and neural ectoderm. This primarily results in the a ... Read the Article | 1 | 6 | Activity DO |
| Holoprosencephaly | Holoprosencephaly occurs as a result of anomalous signaling interactions between the neural crest and neural ectoderm. This primarily results in the a ... Read the Article | 1 | 6 | Activity MD/PA |
| Holt Oram Syndrome | Holt-Oram syndrome also referred to as the heart-hand syndrome, is an autosomal dominant disorder that is distinguished by upper limb abnormalities in ... Read the Article | 1 | 6 | Activity DO |
| Holt Oram Syndrome | Holt-Oram syndrome also referred to as the heart-hand syndrome, is an autosomal dominant disorder that is distinguished by upper limb abnormalities in ... Read the Article | 1 | 6 | Activity MD/PA |
| Hydranencephaly | Hydranencephaly is a rare congenital abnormality in which the cerebral hemispheres are absent with the basal ganglia, brainstem and meninges preserved ... Read the Article | 1 | 5 | Activity DO |
| Hydranencephaly | Hydranencephaly is a rare congenital abnormality in which the cerebral hemispheres are absent with the basal ganglia, brainstem and meninges preserved ... Read the Article | 1 | 5 | Activity MD/PA |
| Hydrocele | A hydrocele is a collection of peritoneal fluid between the parietal and visceral layers of the tunica vaginalis, which directly surrounds the testis ... Read the Article | 1.25 | 9 | Activity DO |
| Hydrocele | A hydrocele is a collection of peritoneal fluid between the parietal and visceral layers of the tunica vaginalis, which directly surrounds the testis ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Hydrocephalus | Hydrocephalus is the symptomatic accumulation of cerebrospinal fluid inside the cerebral ventricles. It has complex pathogenesis and different causes. ... Read the Article | 1.5 | 18 | Activity DO |
| Hydrocephalus | Hydrocephalus is the symptomatic accumulation of cerebrospinal fluid inside the cerebral ventricles. It has complex pathogenesis and different causes. ... Read the Article | 1.5 | 18 | Activity MD/PA |
| Hypermagnesemia | Magnesium is an essential element for the life of plants as it is part of chlorophyll. Moreover, it is abundant in animal tissues, where it is fundame ... Read the Article | 1 | 5 | Activity DO |
| Hypermagnesemia | Magnesium is an essential element for the life of plants as it is part of chlorophyll. Moreover, it is abundant in animal tissues, where it is fundame ... Read the Article | 1 | 5 | Activity MD/PA |
| Hyperthyroidism In Pregnancy | Hyperthyroidism is an uncommon condition that complicates approximately 0.1% to 0.4% of pregnancies. The condition is marked by increased levels of ci ... Read the Article | 1.25 | 7 | Activity DO |
| Hyperthyroidism In Pregnancy | Hyperthyroidism is an uncommon condition that complicates approximately 0.1% to 0.4% of pregnancies. The condition is marked by increased levels of ci ... Read the Article | 1.25 | 7 | Activity MD/PA |
| Hypoaldosteronism | Hypoaldosteronism is a clinical condition characterized by a deficiency of aldosterone or its impaired action at the tissue level. The disorder may re ... Read the Article | 1 | 5 | Activity DO |
| Hypoaldosteronism | Hypoaldosteronism is a clinical condition characterized by a deficiency of aldosterone or its impaired action at the tissue level. The disorder may re ... Read the Article | 1 | 5 | Activity MD/PA |
| Hypocalcemia | Disorders of calcium metabolism are frequently encountered. Though hypocalcemia is not encountered as frequently as hypercalcemia, it can be life-thre ... Read the Article | 1.25 | 11 | Activity DO |
| Hypocalcemia | Disorders of calcium metabolism are frequently encountered. Though hypocalcemia is not encountered as frequently as hypercalcemia, it can be life-thre ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Hypoglycemia | Hypoglycemia is often defined by a plasma glucose concentration below 70 mg/dL; however, signs and symptoms may not occur until plasma glucose concent ... Read the Article | 1.5 | 18 | Activity DO |
| Hypoglycemia | Hypoglycemia is often defined by a plasma glucose concentration below 70 mg/dL; however, signs and symptoms may not occur until plasma glucose concent ... Read the Article | 1.5 | 18 | Activity MD/PA |
| Hypomelanosis of Ito | Hypomelanosis of Ito (HI), or pigmentary mosaicism, was previously named incontinentia pigmenti achromians. The disease is currently named hypomelanos ... Read the Article | 1 | 4 | Activity DO |
| Hypomelanosis of Ito | Hypomelanosis of Ito (HI), or pigmentary mosaicism, was previously named incontinentia pigmenti achromians. The disease is currently named hypomelanos ... Read the Article | 1 | 4 | Activity MD/PA |
| Hypoplastic Left Heart Syndrome | Hypoplastic left heart syndrome (HLHS) is a type of congenital heart disease that results in the underdevelopment of the left-sided structures of the ... Read the Article | 1.25 | 7 | Activity DO |
| Hypoplastic Left Heart Syndrome | Hypoplastic left heart syndrome (HLHS) is a type of congenital heart disease that results in the underdevelopment of the left-sided structures of the ... Read the Article | 1.25 | 7 | Activity MD/PA |
| Hypoplastic Lung Disease | Pulmonary hypoplasia is a relatively uncommon medical condition characterized by incomplete development of the lungs that can affect the overall devel ... Read the Article | 1 | 6 | Activity DO |
| Hypoplastic Lung Disease | Pulmonary hypoplasia is a relatively uncommon medical condition characterized by incomplete development of the lungs that can affect the overall devel ... Read the Article | 1 | 6 | Activity MD/PA |
| Hypospadias | Hypospadias is an anatomical congenital malformation of the male external genitalia. It is characterized by abnormal development of the urethral fold ... Read the Article | 1 | 6 | Activity DO |
| Hypospadias | Hypospadias is an anatomical congenital malformation of the male external genitalia. It is characterized by abnormal development of the urethral fold ... Read the Article | 1 | 6 | Activity MD/PA |
| Hypospadias Urogenital Reconstruction | Hypospadias is one of the most common urogenital anomalies in newborn males. It is defined as the combination of the displacement of the urethral open ... Read the Article | 1 | 6 | Activity DO |
| Hypospadias Urogenital Reconstruction | Hypospadias is one of the most common urogenital anomalies in newborn males. It is defined as the combination of the displacement of the urethral open ... Read the Article | 1 | 6 | Activity MD/PA |
| Hypothalamic Hamartoma | Hypothalamic hamartomas are congenital non-progressive lesions in the hypothalamus. These lesions usually develop a disabling course presenting with m ... Read the Article | 1 | 5 | Activity DO |
| Hypothalamic Hamartoma | Hypothalamic hamartomas are congenital non-progressive lesions in the hypothalamus. These lesions usually develop a disabling course presenting with m ... Read the Article | 1 | 5 | Activity MD/PA |
| Hypothermia | Accidental hypothermia occurs when the body dissipates more heat than it absorbs or creates, leaving the body unable to generate sufficient heat to ma ... Read the Article | 1.5 | 16 | Activity DO |
| Hypothermia | Accidental hypothermia occurs when the body dissipates more heat than it absorbs or creates, leaving the body unable to generate sufficient heat to ma ... Read the Article | 1.5 | 16 | Activity MD/PA |
| Hypotonia | Hypotonia is an easily recognizable entity but determining the etiology is a challenging task for a clinician given its vast differential. Systematica ... Read the Article | 1.25 | 11 | Activity DO |
| Hypotonia | Hypotonia is an easily recognizable entity but determining the etiology is a challenging task for a clinician given its vast differential. Systematica ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Ichthyosis Fetalis | Harlequin ichthyosis (HI) is an extremely rare, autosomal recessive congenital disorder of the epidermal skin layer. Neonates with HI have a high mort ... Read the Article | 1 | 5 | Activity DO |
| Ichthyosis Fetalis | Harlequin ichthyosis (HI) is an extremely rare, autosomal recessive congenital disorder of the epidermal skin layer. Neonates with HI have a high mort ... Read the Article | 1 | 5 | Activity MD/PA |
| Ileal Atresia | Jejunoileal atresia (JIA) is one of the common causes of intestinal obstruction in neonates. It has been generally reported that JIA occurs due to a v ... Read the Article | 1 | 5 | Activity DO |
| Ileal Atresia | Jejunoileal atresia (JIA) is one of the common causes of intestinal obstruction in neonates. It has been generally reported that JIA occurs due to a v ... Read the Article | 1 | 5 | Activity MD/PA |
| Immunodeficiency | Immunodeficiency results from a failure or absence of elements of the immune system, including lymphocytes, phagocytes, and the complement system. Imm ... Read the Article | 1 | 5 | Activity DO |
| Immunodeficiency | Immunodeficiency results from a failure or absence of elements of the immune system, including lymphocytes, phagocytes, and the complement system. Imm ... Read the Article | 1 | 5 | Activity MD/PA |
| Impaired Bilirubin Conjugation | Bilirubin circulates in both the unconjugated and conjugated forms. Disorders of impaired conjugation of bilirubin classically present with elevated l ... Read the Article | 1 | 7 | Activity DO |
| Impaired Bilirubin Conjugation | Bilirubin circulates in both the unconjugated and conjugated forms. Disorders of impaired conjugation of bilirubin classically present with elevated l ... Read the Article | 1 | 7 | Activity MD/PA |
| Imperforate Anus | Imperforate anus or anal atresia is a congenital anorectal malformation (ARM) where a normal anal opening is absent at birth. ARMs comprise of a broad ... Read the Article | 1 | 5 | Activity DO |
| Imperforate Anus | Imperforate anus or anal atresia is a congenital anorectal malformation (ARM) where a normal anal opening is absent at birth. ARMs comprise of a broad ... Read the Article | 1 | 5 | Activity MD/PA |
| Induction of Labor | There are indications for late preterm, early term, late term, and post-term inductions depending on a patient's obstetrical and medical history. Obst ... Read the Article | 1 | 7 | Activity DO |
| Induction of Labor | There are indications for late preterm, early term, late term, and post-term inductions depending on a patient's obstetrical and medical history. Obst ... Read the Article | 1 | 7 | Activity MD/PA |
| Infant Apnea | Apnea in infants is the term used to describe episodes of cessation of breathing and may be due to many physiologic or pathophysiologic processes. Bri ... Read the Article | 1 | 8 | Activity DO |
| Infant Apnea | Apnea in infants is the term used to describe episodes of cessation of breathing and may be due to many physiologic or pathophysiologic processes. Bri ... Read the Article | 1 | 8 | Activity MD/PA |
| Infant Nutrition Requirements and Options | Infancy is a period of rapid growth second only to the fetal period, with a pressing need to optimize nutrition to ensure adequate growth and organ de ... Read the Article | 1.25 | 9 | Activity DO |
| Infant Nutrition Requirements and Options | Infancy is a period of rapid growth second only to the fetal period, with a pressing need to optimize nutrition to ensure adequate growth and organ de ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Infantile Botulism | Infantile botulism is caused by Clostridium botulinum, which is an anaerobic spore-forming, gram-positive bacillus. It can be found in the soil, water ... Read the Article | 1.25 | 11 | Activity DO |
| Infantile Botulism | Infantile botulism is caused by Clostridium botulinum, which is an anaerobic spore-forming, gram-positive bacillus. It can be found in the soil, water ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Infantile Cortical Hyperostosis | Infantile cortical hyperostosis (ICH), also known as Caffey disease, was first reported by Roske in 1930 and described by Caffey and Silverman in 1945 ... Read the Article | 1 | 8 | Activity DO |
| Infantile Cortical Hyperostosis | Infantile cortical hyperostosis (ICH), also known as Caffey disease, was first reported by Roske in 1930 and described by Caffey and Silverman in 1945 ... Read the Article | 1 | 8 | Activity MD/PA |
| Infantile Spasm | Infantile spasms are spasms that occur in infancy or early childhood. They are classically characterized by symmetric, brief jerking spells that invol ... Read the Article | 1 | 5 | Activity DO |
| Infantile Spasm | Infantile spasms are spasms that occur in infancy or early childhood. They are classically characterized by symmetric, brief jerking spells that invol ... Read the Article | 1 | 5 | Activity MD/PA |
| Infantile Spasms | Infantile spasms (IS) is a seizure disorder that was first described by William West in 1841 and has been referred to as West syndrome. It is a disord ... Read the Article | 1 | 6 | Activity DO |
| Infantile Spasms | Infantile spasms (IS) is a seizure disorder that was first described by William West in 1841 and has been referred to as West syndrome. It is a disord ... Read the Article | 1 | 6 | Activity MD/PA |
| Interrupted Aortic Arch | A rare type of congenital heart disease is an interrupted aortic arch (IAA), which affects approximately 1.5% of congenital heart disease patients. In ... Read the Article | 1 | 5 | Activity DO |
| Interrupted Aortic Arch | A rare type of congenital heart disease is an interrupted aortic arch (IAA), which affects approximately 1.5% of congenital heart disease patients. In ... Read the Article | 1 | 5 | Activity MD/PA |
| Intoeing | Deformities and angular variations of the lower extremities are one of the most common reasons for referral to pediatric orthopedics, with in-toeing s ... Read the Article | 1 | 6 | Activity DO |
| Intoeing | Deformities and angular variations of the lower extremities are one of the most common reasons for referral to pediatric orthopedics, with in-toeing s ... Read the Article | 1 | 6 | Activity MD/PA |
| Intraosseous Vascular Access | Obtaining vascular access is often difficult and delays patient care in the prehospital and hospital setting. Intraosseous (IO) access is a fast and r ... Read the Article | 1.25 | 11 | Activity DO |
| Intraosseous Vascular Access | Obtaining vascular access is often difficult and delays patient care in the prehospital and hospital setting. Intraosseous (IO) access is a fast and r ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Intrauterine Fetal Demise | Stillbirth has many causes: intrapartum complications, hypertension, diabetes, infection, congenital and genetic abnormalities, placental dysfunction, ... Read the Article | 1.5 | 6 | Activity DO |
| Intrauterine Fetal Demise | Stillbirth has many causes: intrapartum complications, hypertension, diabetes, infection, congenital and genetic abnormalities, placental dysfunction, ... Read the Article | 1.5 | 6 | Activity MD/PA |
| Jaundice | Jaundice, also known as hyperbilirubinemia, is defined as a yellow discoloration of the body tissue resulting from the accumulation of excess bilirubi ... Read the Article | 1.25 | 12 | Activity DO |
| Jaundice | Jaundice, also known as hyperbilirubinemia, is defined as a yellow discoloration of the body tissue resulting from the accumulation of excess bilirubi ... Read the Article | 1.25 | 12 | Activity MD/PA |
| Junctional Ectopic Tachycardia | Junctional ectopic tachycardia is an arrhythmia usually present in infants but has been seen in older children as well. It can be congenital or postop ... Read the Article | 1 | 4 | Activity DO |
| Junctional Ectopic Tachycardia | Junctional ectopic tachycardia is an arrhythmia usually present in infants but has been seen in older children as well. It can be congenital or postop ... Read the Article | 1 | 4 | Activity MD/PA |
| Kasabach Merritt Syndrome | Kasabach-Merritt phenomenon (KMP), first described in 1940, is a rare but life-threatening coagulopathy of infancy which presents with thrombocytopeni ... Read the Article | 1 | 5 | Activity DO |
| Kasabach Merritt Syndrome | Kasabach-Merritt phenomenon (KMP), first described in 1940, is a rare but life-threatening coagulopathy of infancy which presents with thrombocytopeni ... Read the Article | 1 | 5 | Activity MD/PA |
| Kernicterus | Kernicterus, or bilirubin encephalopathy, is bilirubin-induced neurological damage, which is most commonly seen in infants. It occurs when the unconju ... Read the Article | 1 | 5 | Activity DO |
| Kernicterus | Kernicterus, or bilirubin encephalopathy, is bilirubin-induced neurological damage, which is most commonly seen in infants. It occurs when the unconju ... Read the Article | 1 | 5 | Activity MD/PA |
| Klippel Feil Syndrome | Klippel-Feil syndrome presents with an abnormal fusion of 2 or more bones in the cervical spine. This creates a characteristic appearance of a short n ... Read the Article | 1 | 4 | Activity DO |
| Klippel Feil Syndrome | Klippel-Feil syndrome presents with an abnormal fusion of 2 or more bones in the cervical spine. This creates a characteristic appearance of a short n ... Read the Article | 1 | 4 | Activity MD/PA |
| Klippel Trenaunay Weber Syndrome | Klippel Trenaunay syndrome is cutaneous vascular malformation syndrome involving a triad of capillary and venous malformation and limb hypertrophy. Th ... Read the Article | 1 | 5 | Activity DO |
| Klippel Trenaunay Weber Syndrome | Klippel Trenaunay syndrome is cutaneous vascular malformation syndrome involving a triad of capillary and venous malformation and limb hypertrophy. Th ... Read the Article | 1 | 5 | Activity MD/PA |
| Laryngomalacia | Laryngomalacia ranks as the most prevalent cause of stridor in an infant. It is crucial to make the diagnosis in early infancy as it may affect multip ... Read the Article | 1 | 6 | Activity DO |
| Laryngomalacia | Laryngomalacia ranks as the most prevalent cause of stridor in an infant. It is crucial to make the diagnosis in early infancy as it may affect multip ... Read the Article | 1 | 6 | Activity MD/PA |
| Laxatives | Constipation is a common diagnosis that requires proper evaluation and appropriate treatment. The approach to a patient with chronic constipation incl ... Read the Article | 1 | 5 | Activity DO |
| Laxatives | Constipation is a common diagnosis that requires proper evaluation and appropriate treatment. The approach to a patient with chronic constipation incl ... Read the Article | 1 | 5 | Activity MD/PA |
| Leukocyte Adhesion Deficiency | Leukocyte adhesion deficiency (LAD) is an immunodeficiency disorder involving both B and T cells and is characterized by an inability of leukocytes to ... Read the Article | 1 | 5 | Activity DO |
| Leukocyte Adhesion Deficiency | Leukocyte adhesion deficiency (LAD) is an immunodeficiency disorder involving both B and T cells and is characterized by an inability of leukocytes to ... Read the Article | 1 | 5 | Activity MD/PA |
| Lissencephaly | Lissencephaly is a spectrum of severe and rare brain malformations. It is caused by non-genetic and genetic factors. Treatment of children with lissen ... Read the Article | 1 | 6 | Activity DO |
| Lissencephaly | Lissencephaly is a spectrum of severe and rare brain malformations. It is caused by non-genetic and genetic factors. Treatment of children with lissen ... Read the Article | 1 | 6 | Activity MD/PA |
| Lithium | Despite the availability of newer mood stabilizers, lithium continues to be a first-line treatment for bipolar disorder. It is often underutilized bec ... Read the Article | 1.25 | 9 | Activity DO |
| Lithium | Despite the availability of newer mood stabilizers, lithium continues to be a first-line treatment for bipolar disorder. It is often underutilized bec ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Lymphangioma | Lymphangiomas are uncommon, benign malformations of the lymphatic system that can occur anywhere on the skin and mucous membranes. Lymphangiomas can b ... Read the Article | 1 | 4 | Activity DO |
| Lymphangioma | Lymphangiomas are uncommon, benign malformations of the lymphatic system that can occur anywhere on the skin and mucous membranes. Lymphangiomas can b ... Read the Article | 1 | 4 | Activity MD/PA |
| Lymphedema | Lymphedema is a chronic disease marked by the increased collection of lymphatic fluid in the body, causing swelling, which can lead to skin and tissue ... Read the Article | 1.25 | 10 | Activity DO |
| Lymphedema | Lymphedema is a chronic disease marked by the increased collection of lymphatic fluid in the body, causing swelling, which can lead to skin and tissue ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Macrosomia | Macrosomia is commonly encountered during obstetric practice. It is associated with a higher likelihood of obstetric as well as neonatal complications ... Read the Article | 1 | 4 | Activity DO |
| Macrosomia | Macrosomia is commonly encountered during obstetric practice. It is associated with a higher likelihood of obstetric as well as neonatal complications ... Read the Article | 1 | 4 | Activity MD/PA |
| Mandibulofacial Dysostosis | Treacher Collins syndrome is a congenital disorder of craniofacial development that has variable phenotypic expression. It can be inherited in an auto ... Read the Article | 1 | 5 | Activity DO |
| Mandibulofacial Dysostosis | Treacher Collins syndrome is a congenital disorder of craniofacial development that has variable phenotypic expression. It can be inherited in an auto ... Read the Article | 1 | 5 | Activity MD/PA |
| Maple Syrup Urine Disease | Maple syrup urine disease is a rare, inborn error of metabolism, resulting in decreased branched-chain ketoacid dehydrogenase enzyme activity. It can ... Read the Article | 1 | 6 | Activity DO |
| Maple Syrup Urine Disease | Maple syrup urine disease is a rare, inborn error of metabolism, resulting in decreased branched-chain ketoacid dehydrogenase enzyme activity. It can ... Read the Article | 1 | 6 | Activity MD/PA |
| Marcus Gunn Jaw Winking Syndrome | Marcus Gunn Jaw winking syndrome (MGJWS) is one of the congenital cranial dysinnervation disorders (CCDD) and these individuals have variable degrees ... Read the Article | 1 | 6 | Activity DO |
| Marcus Gunn Jaw Winking Syndrome | Marcus Gunn Jaw winking syndrome (MGJWS) is one of the congenital cranial dysinnervation disorders (CCDD) and these individuals have variable degrees ... Read the Article | 1 | 6 | Activity MD/PA |
| Marijuana And Maternal, Perinatal, and Neonatal Outcomes | Drug use and drug dependency are major public health problems. Marijuana is one of the most commonly used drugs among all genders and age groups. This ... Read the Article | 1 | 5 | Activity DO |
| Marijuana And Maternal, Perinatal, and Neonatal Outcomes | Drug use and drug dependency are major public health problems. Marijuana is one of the most commonly used drugs among all genders and age groups. This ... Read the Article | 1 | 5 | Activity MD/PA |
| Meconium Aspiration | Meconium aspiration syndrome (MAS) is the neonatal respiratory distress that occurs in a newborn in the context of meconium-stained amniotic fluid (MA ... Read the Article | 1 | 4 | Activity DO |
| Meconium Aspiration | Meconium aspiration syndrome (MAS) is the neonatal respiratory distress that occurs in a newborn in the context of meconium-stained amniotic fluid (MA ... Read the Article | 1 | 4 | Activity MD/PA |
| Meconium Ileus | Meconium Ileus (MI) is one of the earliest manifestations of cystic fibrosis (CF) and presents in up to 20 percent of infants with CF. The inspissated ... Read the Article | 1 | 5 | Activity DO |
| Meconium Ileus | Meconium Ileus (MI) is one of the earliest manifestations of cystic fibrosis (CF) and presents in up to 20 percent of infants with CF. The inspissated ... Read the Article | 1 | 5 | Activity MD/PA |
| Meconium Plug Syndrome | Meconium plug syndrome is a condition that predominantly affects preterm-neonates of low birth weight. It presents with an inability to pass meconium ... Read the Article | 1 | 5 | Activity DO |
| Meconium Plug Syndrome | Meconium plug syndrome is a condition that predominantly affects preterm-neonates of low birth weight. It presents with an inability to pass meconium ... Read the Article | 1 | 5 | Activity MD/PA |
| Medium-Chain Acyl-COA Dehydrogenase Deficiency | Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is one of the most common fatty acid ß-oxidation disorders. It is an autosomal recessive disorde ... Read the Article | 1 | 6 | Activity DO |
| Medium-Chain Acyl-COA Dehydrogenase Deficiency | Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is one of the most common fatty acid ß-oxidation disorders. It is an autosomal recessive disorde ... Read the Article | 1 | 6 | Activity MD/PA |
| Meningitis | In spite of breakthroughs in diagnosis, treatment, and vaccination, in 2015 there were 8.7 million reported cases of meningitis worldwide with 379,000 ... Read the Article | 1.25 | 13 | Activity DO |
| Meningitis | In spite of breakthroughs in diagnosis, treatment, and vaccination, in 2015 there were 8.7 million reported cases of meningitis worldwide with 379,000 ... Read the Article | 1.25 | 13 | Activity MD/PA |
| Meningocele | Meningocele is one of the common congenital neural tube defects. Meningocele is the simplest form of open neural tube defects characterized by cystic ... Read the Article | 1.5 | 14 | Activity DO |
| Meningocele | Meningocele is one of the common congenital neural tube defects. Meningocele is the simplest form of open neural tube defects characterized by cystic ... Read the Article | 1.5 | 14 | Activity MD/PA |
| Meningomyelocele | Myelomeningocele or open spina bifida is a devastating congenital malformation of the central nervous system associated with significant morbidity. Ti ... Read the Article | 1 | 7 | Activity DO |
| Meningomyelocele | Myelomeningocele or open spina bifida is a devastating congenital malformation of the central nervous system associated with significant morbidity. Ti ... Read the Article | 1 | 7 | Activity MD/PA |
| Menkes Kinky Hair Disease | Menkes kinky hair disease is a rare X-linked recessive progressive multisystemic disease of copper metabolism. Patients usually exhibit a severe clini ... Read the Article | 1 | 6 | Activity DO |
| Menkes Kinky Hair Disease | Menkes kinky hair disease is a rare X-linked recessive progressive multisystemic disease of copper metabolism. Patients usually exhibit a severe clini ... Read the Article | 1 | 6 | Activity MD/PA |
| Meromelia | Meromelia is defined as a partial absence of a free limb. Limb deficiencies have been known to be caused by chromosomal abnormalities, genetic disorde ... Read the Article | 1 | 5 | Activity DO |
| Meromelia | Meromelia is defined as a partial absence of a free limb. Limb deficiencies have been known to be caused by chromosomal abnormalities, genetic disorde ... Read the Article | 1 | 5 | Activity MD/PA |
| Methemoglobinemia | Methemoglobinemia is a condition with life-threatening potential in which diminution of the oxygen-carrying capacity of circulating hemoglobin occurs ... Read the Article | 1 | 6 | Activity DO |
| Methemoglobinemia | Methemoglobinemia is a condition with life-threatening potential in which diminution of the oxygen-carrying capacity of circulating hemoglobin occurs ... Read the Article | 1 | 6 | Activity MD/PA |
| Micropenis | Micropenis is a vital sign that can indicate a hormonal deficiency or genetic association. Early recognition of this condition is essential in providi ... Read the Article | 1 | 4 | Activity DO |
| Micropenis | Micropenis is a vital sign that can indicate a hormonal deficiency or genetic association. Early recognition of this condition is essential in providi ... Read the Article | 1 | 4 | Activity MD/PA |
| Midgut Malrotation | Midgut malrotation is a defect in the normal embryonic rotation of the gut, which causes an abdominal obstruction that presents acutely or with chroni ... Read the Article | 1 | 4 | Activity DO |
| Midgut Malrotation | Midgut malrotation is a defect in the normal embryonic rotation of the gut, which causes an abdominal obstruction that presents acutely or with chroni ... Read the Article | 1 | 4 | Activity MD/PA |
| Midgut Volvulus | A volvulus is a medical condition where the intestines twist upon themselves. This condition can occur at any age. However, it is more frequent in chi ... Read the Article | 1.25 | 8 | Activity DO |
| Midgut Volvulus | A volvulus is a medical condition where the intestines twist upon themselves. This condition can occur at any age. However, it is more frequent in chi ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Milia | Milia are benign and transient dermal cysts of keratine. These white appearing bumps are common, present in many different ways, and can develop in an ... Read the Article | 1 | 6 | Activity DO |
| Milia | Milia are benign and transient dermal cysts of keratine. These white appearing bumps are common, present in many different ways, and can develop in an ... Read the Article | 1 | 6 | Activity MD/PA |
| Miliaria | Miliaria, also known as eccrine miliaria, heat rash, prickly heat, or sweat rash, is a frequently seen skin condition triggered by blocked eccrine swe ... Read the Article | 1 | 5 | Activity DO |
| Miliaria | Miliaria, also known as eccrine miliaria, heat rash, prickly heat, or sweat rash, is a frequently seen skin condition triggered by blocked eccrine swe ... Read the Article | 1 | 5 | Activity MD/PA |
| Mitral Stenosis | Mitral stenosis (MS) is a form of valvular heart disease characterized by narrowing of the mitral valve orifice. The most common cause of mitral steno ... Read the Article | 2.25 | 34 | Activity DO |
| Mitral Stenosis | Mitral stenosis (MS) is a form of valvular heart disease characterized by narrowing of the mitral valve orifice. The most common cause of mitral steno ... Read the Article | 2.25 | 34 | Activity MD/PA |
| Myelomeningocele | Neural tube defects are a spectrum of congenital anomalies that includes cranial defects and open or closed spinal dysraphism. Open spinal dysraphism ... Read the Article | 1.25 | 10 | Activity DO |
| Myelomeningocele | Neural tube defects are a spectrum of congenital anomalies that includes cranial defects and open or closed spinal dysraphism. Open spinal dysraphism ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Nasolacrimal Duct Obstruction | Nasolacrimal duct obstruction (NLDO) or dacryostenosis is the most common disorder of the lacrimal system, and approximately 6 to 20 percent of newbor ... Read the Article | 1 | 5 | Activity DO |
| Nasolacrimal Duct Obstruction | Nasolacrimal duct obstruction (NLDO) or dacryostenosis is the most common disorder of the lacrimal system, and approximately 6 to 20 percent of newbor ... Read the Article | 1 | 5 | Activity MD/PA |
| Necrotizing Enterocolitis | Necrotizing enterocolitis (NEC) is a life-threatening illness almost exclusively affecting neonates with a mortality rate as high as 50 percent. The p ... Read the Article | 1 | 7 | Activity DO |
| Necrotizing Enterocolitis | Necrotizing enterocolitis (NEC) is a life-threatening illness almost exclusively affecting neonates with a mortality rate as high as 50 percent. The p ... Read the Article | 1 | 7 | Activity MD/PA |
| Neonatal Abstinence Syndrome | Neonatal Abstinence Syndrome (NAS) is a spectrum of clinical manifestations seen in neonates due to withdrawal from intrauterine drug exposure. It is ... Read the Article | 1.25 | 6 | Activity DO |
| Neonatal Abstinence Syndrome | Neonatal Abstinence Syndrome (NAS) is a spectrum of clinical manifestations seen in neonates due to withdrawal from intrauterine drug exposure. It is ... Read the Article | 1.25 | 6 | Activity MD/PA |
| Neonatal Conjunctivitis | Neonatal eye discharge is usually due to congenital nasolacrimal duct obstruction or either chemical or infectious conjunctivitis. Neonatal conjunctiv ... Read the Article | 1 | 6 | Activity DO |
| Neonatal Conjunctivitis | Neonatal eye discharge is usually due to congenital nasolacrimal duct obstruction or either chemical or infectious conjunctivitis. Neonatal conjunctiv ... Read the Article | 1 | 6 | Activity MD/PA |
| Neonatal EEG | Neurological evaluation of the neonate has many inherent limitations that make it challenging to delineate physiological variations from pathological ... Read the Article | 1 | 5 | Activity DO |
| Neonatal EEG | Neurological evaluation of the neonate has many inherent limitations that make it challenging to delineate physiological variations from pathological ... Read the Article | 1 | 5 | Activity MD/PA |
| Neonatal Evaluation | The initial examination within the first 24 hours of birth is critical in determining newborns' general well-being and identifying any red flags that ... Read the Article | 1.25 | 7 | Activity DO |
| Neonatal Evaluation | The initial examination within the first 24 hours of birth is critical in determining newborns' general well-being and identifying any red flags that ... Read the Article | 1.25 | 7 | Activity MD/PA |
| Neonatal HIV | Over 95% of HIV-infected pediatric cases are a result of vertical transmission. Neonatal HIV is the concern for HIV in an infant born to a mother with ... Read the Article | 1 | 5 | Activity DO |
| Neonatal HIV | Over 95% of HIV-infected pediatric cases are a result of vertical transmission. Neonatal HIV is the concern for HIV in an infant born to a mother with ... Read the Article | 1 | 5 | Activity MD/PA |
| Neonatal Hyperglycemia | Hyperglycemia is less common than hypoglycemia among neonates, but it is essential to address it because it increases mortality and morbidity among ne ... Read the Article | 1 | 5 | Activity DO |
| Neonatal Hyperglycemia | Hyperglycemia is less common than hypoglycemia among neonates, but it is essential to address it because it increases mortality and morbidity among ne ... Read the Article | 1 | 5 | Activity MD/PA |
| Neonatal Hypertension | Neonatal hypertension often has non-specific presentation and it is commonly under-diagnosed. However, in the last few years, with the advancing techn ... Read the Article | 1 | 6 | Activity DO |
| Neonatal Hypertension | Neonatal hypertension often has non-specific presentation and it is commonly under-diagnosed. However, in the last few years, with the advancing techn ... Read the Article | 1 | 6 | Activity MD/PA |
| Neonatal Hypoglycemia | Hypoglycemia is the most common metabolic disturbance occurring in the neonatal period. Screening at-risk infants and the management of low blood gluc ... Read the Article | 1 | 2 | Activity DO |
| Neonatal Hypoglycemia | Hypoglycemia is the most common metabolic disturbance occurring in the neonatal period. Screening at-risk infants and the management of low blood gluc ... Read the Article | 1 | 2 | Activity MD/PA |
| Neonatal Jaundice | Neonatal jaundice is yellowish discoloration of the skin, conjunctiva, and sclera due to elevated serum or plasma bilirubin in the newborn period. Neo ... Read the Article | 1.25 | 7 | Activity DO |
| Neonatal Jaundice | Neonatal jaundice is yellowish discoloration of the skin, conjunctiva, and sclera due to elevated serum or plasma bilirubin in the newborn period. Neo ... Read the Article | 1.25 | 7 | Activity MD/PA |
| Neonatal Lupus Erythematosus | Neonatal lupus erythematosus is an autoimmune disease that takes place due to the passive maternal transfer of autoantibodies of Sjogren syndrome auto ... Read the Article | 1 | 7 | Activity DO |
| Neonatal Lupus Erythematosus | Neonatal lupus erythematosus is an autoimmune disease that takes place due to the passive maternal transfer of autoantibodies of Sjogren syndrome auto ... Read the Article | 1 | 7 | Activity MD/PA |
| Neonatal Meningitis | Bacterial meningitis during the neonatal period remains a highly devastating condition, with a morbidity rate of 20 to 60 percent. The nationwide mort ... Read the Article | 1 | 7 | Activity DO |
| Neonatal Meningitis | Bacterial meningitis during the neonatal period remains a highly devastating condition, with a morbidity rate of 20 to 60 percent. The nationwide mort ... Read the Article | 1 | 7 | Activity MD/PA |
| Neonatal Myasthenia Gravis | Neonatal myasthenia gravis (MG) is a temporary form of MG. Babies born to mothers with MG are susceptible to it. This is due to the mother’s antibodi ... Read the Article | 1 | 5 | Activity DO |
| Neonatal Myasthenia Gravis | Neonatal myasthenia gravis (MG) is a temporary form of MG. Babies born to mothers with MG are susceptible to it. This is due to the mother’s antibodi ... Read the Article | 1 | 5 | Activity MD/PA |
| Neonatal Respiratory Distress Syndrome | Neonatal respiratory distress syndrome is a frequent cause of increased morbidity and mortality in neonates. Understanding the pathophysiology, clinic ... Read the Article | 1.5 | 14 | Activity DO |
| Neonatal Respiratory Distress Syndrome | Neonatal respiratory distress syndrome is a frequent cause of increased morbidity and mortality in neonates. Understanding the pathophysiology, clinic ... Read the Article | 1.5 | 14 | Activity MD/PA |
| Neonatal Seizure | Neonatal seizures are a commonly encountered neurologic condition in neonates. They are defined as the occurrence of sudden, paroxysmal, abnormal alte ... Read the Article | 1.5 | 14 | Activity DO |
| Neonatal Seizure | Neonatal seizures are a commonly encountered neurologic condition in neonates. They are defined as the occurrence of sudden, paroxysmal, abnormal alte ... Read the Article | 1.5 | 14 | Activity MD/PA |
| Neonatal Sepsis | Neonatal sepsis refers to an infection involving bloodstream in newborn infants less than 28 days old. It continues to remain a leading cause of morbi ... Read the Article | 1.25 | 8 | Activity DO |
| Neonatal Sepsis | Neonatal sepsis refers to an infection involving bloodstream in newborn infants less than 28 days old. It continues to remain a leading cause of morbi ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Neonatal Therapeutic Hypothermia | Hypoxic-ischemic encephalopathy among neonates is a significant cause of infant mortality and neurodevelopmental deficits. It is evident from many sys ... Read the Article | 1 | 5 | Activity DO |
| Neonatal Therapeutic Hypothermia | Hypoxic-ischemic encephalopathy among neonates is a significant cause of infant mortality and neurodevelopmental deficits. It is evident from many sys ... Read the Article | 1 | 5 | Activity MD/PA |
| Neural Tube Disorders | Neural tube defects are the most common severe central nervous system anomalies, only second to cardiovascular abnormalities resulting in congenital m ... Read the Article | 1.5 | 13 | Activity DO |
| Neural Tube Disorders | Neural tube defects are the most common severe central nervous system anomalies, only second to cardiovascular abnormalities resulting in congenital m ... Read the Article | 1.5 | 13 | Activity MD/PA |
| Neurally Adjusted Ventilatory Assist (NAVA) | Neurally-adjusted ventilatory assist (NAVA) is a relatively newer mode of ventilation in which a ventilator utilizes the electrical activity of the di ... Read the Article | 1 | 5 | Activity DO |
| Neurally Adjusted Ventilatory Assist (NAVA) | Neurally-adjusted ventilatory assist (NAVA) is a relatively newer mode of ventilation in which a ventilator utilizes the electrical activity of the di ... Read the Article | 1 | 5 | Activity MD/PA |
| Neurosonography Assessment, Protocols, And Interpretation | Several congenital and acquired brain pathologies can be seen in infants. Ultrasound is an excellent initial imaging modality used for the assessment ... Read the Article | 1.25 | 8 | Activity DO |
| Neurosonography Assessment, Protocols, And Interpretation | Several congenital and acquired brain pathologies can be seen in infants. Ultrasound is an excellent initial imaging modality used for the assessment ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Neurosyphilis | With the advent of antibiotics, neurosyphilis became a rare diagnosis. However, syphilis has recently made a resurgence because untreated neurosyphili ... Read the Article | 1.25 | 9 | Activity DO |
| Neurosyphilis | With the advent of antibiotics, neurosyphilis became a rare diagnosis. However, syphilis has recently made a resurgence because untreated neurosyphili ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Newborn Subcutaneous Fat Necrosis | Subcutaneous fat necrosis of the newborn is a rare, self-limited panniculitis that typically occurs in full-term or post-term newborn infants within t ... Read the Article | 1 | 7 | Activity DO |
| Newborn Subcutaneous Fat Necrosis | Subcutaneous fat necrosis of the newborn is a rare, self-limited panniculitis that typically occurs in full-term or post-term newborn infants within t ... Read the Article | 1 | 7 | Activity MD/PA |
| Nitric Oxide | Nitric oxide is a medication used to manage and treat hypoxic respiratory failure or persistent pulmonary hypertension of the newborn (PPHN). It is in ... Read the Article | 1.25 | 8 | Activity DO |
| Nitric Oxide | Nitric oxide is a medication used to manage and treat hypoxic respiratory failure or persistent pulmonary hypertension of the newborn (PPHN). It is in ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Nitrofurantoin | Nitrofurantoin is an antibiotic medication that is used for the treatment of uncomplicated lower urinary tract infection. It is effective against most ... Read the Article | 1 | 6 | Activity DO |
| Nitrofurantoin | Nitrofurantoin is an antibiotic medication that is used for the treatment of uncomplicated lower urinary tract infection. It is effective against most ... Read the Article | 1 | 6 | Activity MD/PA |
| Nonketotic Hyperglycinemia | Nonketotic hyperglycinemia is a rare, genetic, inborn error of glycine metabolism. Due to a mutation in the glycine cleavage enzyme system, the patien ... Read the Article | 1 | 5 | Activity DO |
| Nonketotic Hyperglycinemia | Nonketotic hyperglycinemia is a rare, genetic, inborn error of glycine metabolism. Due to a mutation in the glycine cleavage enzyme system, the patien ... Read the Article | 1 | 5 | Activity MD/PA |
| Noonan Syndrome | Noonan syndrome is typically a genetically inherited disorder with heterogeneous phenotypic manifestations that can change with age. The most consiste ... Read the Article | 1 | 6 | Activity DO |
| Noonan Syndrome | Noonan syndrome is typically a genetically inherited disorder with heterogeneous phenotypic manifestations that can change with age. The most consiste ... Read the Article | 1 | 6 | Activity MD/PA |
| Nuclear Medicine Pediatric Assessment, Protocols, And Interpretation | Nuclear medicine and other radiological techniques impart some ionizing radiation exposure to patients. Within the pediatric population, the disease d ... Read the Article | 1.25 | 6 | Activity DO |
| Nuclear Medicine Pediatric Assessment, Protocols, And Interpretation | Nuclear medicine and other radiological techniques impart some ionizing radiation exposure to patients. Within the pediatric population, the disease d ... Read the Article | 1.25 | 6 | Activity MD/PA |
| Ochronosis | Ochronosis is named for the reddish-brown hue of tissue termed "ochre-like" that was first described by a young physician named Archibald Garrod in th ... Read the Article | 1 | 5 | Activity DO |
| Ochronosis | Ochronosis is named for the reddish-brown hue of tissue termed "ochre-like" that was first described by a young physician named Archibald Garrod in th ... Read the Article | 1 | 5 | Activity MD/PA |
| Omphalitis | Omphalitis is an infection of the umbilicus and/or surrounding tissues, occurring primarily in the neonatal period. It is a true medical emergency tha ... Read the Article | 1 | 6 | Activity DO |
| Omphalitis | Omphalitis is an infection of the umbilicus and/or surrounding tissues, occurring primarily in the neonatal period. It is a true medical emergency tha ... Read the Article | 1 | 6 | Activity MD/PA |
| Omphalocele | Omphalocele is a rare congenital abdominal wall defect with a reported prevalence of 3.38 per 10,000 pregnancies. It is a protrusion of the abdominal ... Read the Article | 1 | 4 | Activity DO |
| Omphalocele | Omphalocele is a rare congenital abdominal wall defect with a reported prevalence of 3.38 per 10,000 pregnancies. It is a protrusion of the abdominal ... Read the Article | 1 | 4 | Activity MD/PA |
| Ophthalmia Neonatorum | Ophthalmia neonatorum is a type of conjunctivitis that takes place in the neonatal period. This condition is commonly transmitted during vaginal deliv ... Read the Article | 1 | 6 | Activity DO |
| Ophthalmia Neonatorum | Ophthalmia neonatorum is a type of conjunctivitis that takes place in the neonatal period. This condition is commonly transmitted during vaginal deliv ... Read the Article | 1 | 6 | Activity MD/PA |
| Optic Nerve Coloboma | The term coloboma derives from the Greek word koloboma, originally used to indicate a part that was removed by mutilation, missing or cut short. Colob ... Read the Article | 1 | 5 | Activity DO |
| Optic Nerve Coloboma | The term coloboma derives from the Greek word koloboma, originally used to indicate a part that was removed by mutilation, missing or cut short. Colob ... Read the Article | 1 | 5 | Activity MD/PA |
| Ornithine Transcarbamylase Deficiency | Ornithine transcarbamylase deficiency is the most common of the urea cycle disorders. It is an X-linked genetic disorder that prevents the breakdown a ... Read the Article | 1 | 4 | Activity DO |
| Ornithine Transcarbamylase Deficiency | Ornithine transcarbamylase deficiency is the most common of the urea cycle disorders. It is an X-linked genetic disorder that prevents the breakdown a ... Read the Article | 1 | 4 | Activity MD/PA |
| Oropharyngeal Airway | Acute respiratory failure is caused by a wide range of etiologies. Progression to cardiopulmonary arrest and ultimately death is likely in the absenc ... Read the Article | 1 | 4 | Activity DO |
| Oropharyngeal Airway | Acute respiratory failure is caused by a wide range of etiologies. Progression to cardiopulmonary arrest and ultimately death is likely in the absenc ... Read the Article | 1 | 4 | Activity MD/PA |
| Osteogenesis Imperfecta | Osteogenesis imperfecta (OI) is a genetic disorder of connective tissues caused by an abnormality in the synthesis or processing of type I collagen. I ... Read the Article | 1.25 | 11 | Activity DO |
| Osteogenesis Imperfecta | Osteogenesis imperfecta (OI) is a genetic disorder of connective tissues caused by an abnormality in the synthesis or processing of type I collagen. I ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Otitis Media With Effusion | Otitis media with effusion (OME) is a condition in which there is fluid in the middle ear, but no signs of acute infection. As fluid builds up in the ... Read the Article | 1 | 5 | Activity DO |
| Otitis Media With Effusion | Otitis media with effusion (OME) is a condition in which there is fluid in the middle ear, but no signs of acute infection. As fluid builds up in the ... Read the Article | 1 | 5 | Activity MD/PA |
| Oxygen Toxicity | Oxygen is vital to sustaining life. However, breathing oxygen at higher than normal partial pressure leads to hyperoxia and can cause oxygen toxicity ... Read the Article | 1 | 6 | Activity DO |
| Oxygen Toxicity | Oxygen is vital to sustaining life. However, breathing oxygen at higher than normal partial pressure leads to hyperoxia and can cause oxygen toxicity ... Read the Article | 1 | 6 | Activity MD/PA |
| Parental Consent | Physicians and medical researchers have a moral and legal obligation to obtain informed consent. Informed consent must include the patient being compe ... Read the Article | 1 | 5 | Activity DO |
| Parental Consent | Physicians and medical researchers have a moral and legal obligation to obtain informed consent. Informed consent must include the patient being compe ... Read the Article | 1 | 5 | Activity MD/PA |
| Partial And Total Anomalous Pulmonary Venous Connection | Total and partial anomalous venous connection comprises a wide spectrum of congenital cardiovascular malformations where one or more pulmonary veins r ... Read the Article | 1 | 6 | Activity DO |
| Partial And Total Anomalous Pulmonary Venous Connection | Total and partial anomalous venous connection comprises a wide spectrum of congenital cardiovascular malformations where one or more pulmonary veins r ... Read the Article | 1 | 6 | Activity MD/PA |
| Parvoviruses | Parvovirus B19 is a virus that only infects humans. It is known to cause fifth disease, also known as erythema infectiosum or slapped cheek syndrome, ... Read the Article | 1 | 5 | Activity DO |
| Parvoviruses | Parvovirus B19 is a virus that only infects humans. It is known to cause fifth disease, also known as erythema infectiosum or slapped cheek syndrome, ... Read the Article | 1 | 5 | Activity MD/PA |
| Patau Syndrome | Patau syndrome, also called trisomy 13, is a clinical syndrome that occurs when all or some cells of the body contain an extra copy of chromosome 13. ... Read the Article | 1 | 5 | Activity DO |
| Patau Syndrome | Patau syndrome, also called trisomy 13, is a clinical syndrome that occurs when all or some cells of the body contain an extra copy of chromosome 13. ... Read the Article | 1 | 5 | Activity MD/PA |
| Patent Ductus Arteriosus | The ductus arteriosus is a fetal vessel that allows the oxygenated blood from the placenta to bypass the fetal lungs in utero. At birth, a newborn inh ... Read the Article | 1.75 | 24 | Activity DO |
| Patent Ductus Arteriosus | The ductus arteriosus is a fetal vessel that allows the oxygenated blood from the placenta to bypass the fetal lungs in utero. At birth, a newborn inh ... Read the Article | 1.75 | 24 | Activity MD/PA |
| Patent Foramen Ovale | Patent foramen ovale (PFO) occurs when a remnant of normal fetal anatomy abnormally persists into adulthood. It represents a benign finding in the new ... Read the Article | 1 | 5 | Activity DO |
| Patent Foramen Ovale | Patent foramen ovale (PFO) occurs when a remnant of normal fetal anatomy abnormally persists into adulthood. It represents a benign finding in the new ... Read the Article | 1 | 5 | Activity MD/PA |
| Patent Urachus | Patent urachus refers to a spectrum of umbilical disorders that result from the failure of involution of normal embryologic tissues that connect the d ... Read the Article | 1 | 5 | Activity DO |
| Patent Urachus | Patent urachus refers to a spectrum of umbilical disorders that result from the failure of involution of normal embryologic tissues that connect the d ... Read the Article | 1 | 5 | Activity MD/PA |
| Pediatric Abusive Head Trauma | Pediatric abusive head trauma (AHT), or shaken baby syndrome, most often involves shaking, blunt impact, or a combination of both in infants and young ... Read the Article | 2 | 24 | Activity DO |
| Pediatric Abusive Head Trauma | Pediatric abusive head trauma (AHT), or shaken baby syndrome, most often involves shaking, blunt impact, or a combination of both in infants and young ... Read the Article | 2 | 24 | Activity MD/PA |
| Pediatric And Neonatal Resuscitation | Cardiopulmonary resuscitation is a sequential algorithm that is the basis of achieving the return of spontaneous circulation. While pediatric patients ... Read the Article | 1.25 | 8 | Activity DO |
| Pediatric And Neonatal Resuscitation | Cardiopulmonary resuscitation is a sequential algorithm that is the basis of achieving the return of spontaneous circulation. While pediatric patients ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Pediatric Bronchiolitis | Bronchiolitis is inflammation of the bronchioles usually caused by an acute viral illness. It is the most common lower respiratory tract infection in ... Read the Article | 1 | 8 | Activity DO |
| Pediatric Bronchiolitis | Bronchiolitis is inflammation of the bronchioles usually caused by an acute viral illness. It is the most common lower respiratory tract infection in ... Read the Article | 1 | 8 | Activity MD/PA |
| Pediatric Cataract | A pediatric cataract is an important cause of treatable childhood blindness, provided it is recognized and managed early. Leukocoria, strabismus, and ... Read the Article | 1.25 | 9 | Activity DO |
| Pediatric Cataract | A pediatric cataract is an important cause of treatable childhood blindness, provided it is recognized and managed early. Leukocoria, strabismus, and ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Pediatric Fluid Management | Dehydration occurs commonly in children and many times requires resuscitation. Fluid resuscitation is essential in the management of critically ill ch ... Read the Article | 1.25 | 12 | Activity DO |
| Pediatric Fluid Management | Dehydration occurs commonly in children and many times requires resuscitation. Fluid resuscitation is essential in the management of critically ill ch ... Read the Article | 1.25 | 12 | Activity MD/PA |
| Pediatric Functional Constipation | Most individuals have bowel movements at regular intervals, and although the frequency varies from person to person, stools should pass without signif ... Read the Article | 1 | 5 | Activity DO |
| Pediatric Functional Constipation | Most individuals have bowel movements at regular intervals, and although the frequency varies from person to person, stools should pass without signif ... Read the Article | 1 | 5 | Activity MD/PA |
| Pediatric Pneumonia | Globally, pneumonia is a leading cause of morbidity and mortality in children younger than the age of 5 years. Although the majority of deaths attribu ... Read the Article | 1.25 | 8 | Activity DO |
| Pediatric Pneumonia | Globally, pneumonia is a leading cause of morbidity and mortality in children younger than the age of 5 years. Although the majority of deaths attribu ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Pediatric Umbilical Hernia | An umbilical hernia presents as a bulge at the site of the umbilicus; it is a common finding during routine well-baby visits for the first few months ... Read the Article | 1 | 7 | Activity DO |
| Pediatric Umbilical Hernia | An umbilical hernia presents as a bulge at the site of the umbilicus; it is a common finding during routine well-baby visits for the first few months ... Read the Article | 1 | 7 | Activity MD/PA |
| Pelvic Kidney | The term pelvic kidney encompasses a range of anatomical abnormalities that occur when the kidney fails to rise from the pelvis in its metanephros sta ... Read the Article | 1 | 4 | Activity DO |
| Pelvic Kidney | The term pelvic kidney encompasses a range of anatomical abnormalities that occur when the kidney fails to rise from the pelvis in its metanephros sta ... Read the Article | 1 | 4 | Activity MD/PA |
| Pentalogy of Cantrell | Pentalogy of Cantrell is a collection of congenital malformations involving the heart, pericardium, diaphragm, sternum, and ventral abdominal wall. It ... Read the Article | 1 | 4 | Activity DO |
| Pentalogy of Cantrell | Pentalogy of Cantrell is a collection of congenital malformations involving the heart, pericardium, diaphragm, sternum, and ventral abdominal wall. It ... Read the Article | 1 | 4 | Activity MD/PA |
| Perimortem Cesarean | The perimortem cesarean section, as described in its name, is the surgical delivery of the fetus, performed during or near the time of death of the mo ... Read the Article | 1 | 5 | Activity DO |
| Perimortem Cesarean | The perimortem cesarean section, as described in its name, is the surgical delivery of the fetus, performed during or near the time of death of the mo ... Read the Article | 1 | 5 | Activity MD/PA |
| Perinatal Drug Abuse And Neonatal Drug Withdrawal | Drug abuse and addiction have significantly increased over the last few decades; specifically, opioid abuse and dependence have increased to epidemic ... Read the Article | 1 | 5 | Activity DO |
| Perinatal Drug Abuse And Neonatal Drug Withdrawal | Drug abuse and addiction have significantly increased over the last few decades; specifically, opioid abuse and dependence have increased to epidemic ... Read the Article | 1 | 5 | Activity MD/PA |
| Periventricular Hemorrhage-Intraventricular Hemorrhage | Periventricular-intraventricular hemorrhage is a disease process that primarily affects the premature newborn infant born at less than 33 weeks of ges ... Read the Article | 1.25 | 8 | Activity DO |
| Periventricular Hemorrhage-Intraventricular Hemorrhage | Periventricular-intraventricular hemorrhage is a disease process that primarily affects the premature newborn infant born at less than 33 weeks of ges ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Pfeiffer Syndrome | Pfeiffer syndrome is an inherited craniofacial disorder that is associated with primary craniosynostosis, midface hypoplasia, broad thumbs and great t ... Read the Article | 1 | 6 | Activity DO |
| Pfeiffer Syndrome | Pfeiffer syndrome is an inherited craniofacial disorder that is associated with primary craniosynostosis, midface hypoplasia, broad thumbs and great t ... Read the Article | 1 | 6 | Activity MD/PA |
| PHACE Syndrome | Infantile hemangioma is the most prevalent benign tumor of infancy, with an estimated incidence between 4 and 5 percent. Large facial segmental hemang ... Read the Article | 1 | 7 | Activity DO |
| PHACE Syndrome | Infantile hemangioma is the most prevalent benign tumor of infancy, with an estimated incidence between 4 and 5 percent. Large facial segmental hemang ... Read the Article | 1 | 7 | Activity MD/PA |
| Phenylketonuria | Phenylketonuria (PKU) is an inborn error of metabolism (IEM) most often caused by missense mutations in the gene encoding phenylalanine hydroxylase (P ... Read the Article | 1.25 | 13 | Activity DO |
| Phenylketonuria | Phenylketonuria (PKU) is an inborn error of metabolism (IEM) most often caused by missense mutations in the gene encoding phenylalanine hydroxylase (P ... Read the Article | 1.25 | 13 | Activity MD/PA |
| Phocomelia | Phocomelia is a rare congenital anomaly where the proximal aspect of an extremity is absent with the hand or foot attached directly to the trunk. This ... Read the Article | 1 | 5 | Activity DO |
| Phocomelia | Phocomelia is a rare congenital anomaly where the proximal aspect of an extremity is absent with the hand or foot attached directly to the trunk. This ... Read the Article | 1 | 5 | Activity MD/PA |
| Phrenic Nerve Injury | The phrenic nerve is among the most important nerves in the body due to its role in respiration. The phrenic nerve provides the primary motor supply t ... Read the Article | 1.25 | 9 | Activity DO |
| Phrenic Nerve Injury | The phrenic nerve is among the most important nerves in the body due to its role in respiration. The phrenic nerve provides the primary motor supply t ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Pierre Robin Syndrome | Pierre Robin sequence is a constellation of micrognathia, glossoptosis, and upper airway obstruction. It is a clinical diagnosis that can range in sev ... Read the Article | 1 | 5 | Activity DO |
| Pierre Robin Syndrome | Pierre Robin sequence is a constellation of micrognathia, glossoptosis, and upper airway obstruction. It is a clinical diagnosis that can range in sev ... Read the Article | 1 | 5 | Activity MD/PA |
| Plagiocephaly | Plagiocephaly is defined as an asymmetric shape of the head due to unilateral flattening. The term flathead can be used as a synonym. Plagiocephaly ca ... Read the Article | 1 | 6 | Activity DO |
| Plagiocephaly | Plagiocephaly is defined as an asymmetric shape of the head due to unilateral flattening. The term flathead can be used as a synonym. Plagiocephaly ca ... Read the Article | 1 | 6 | Activity MD/PA |
| Pneumatocele | Pneumatoceles are air-filled cavitary lesions usually seen in the lung after infection, trauma, or as a part of more extensive cystic disease of the l ... Read the Article | 1.25 | 6 | Activity DO |
| Pneumatocele | Pneumatoceles are air-filled cavitary lesions usually seen in the lung after infection, trauma, or as a part of more extensive cystic disease of the l ... Read the Article | 1.25 | 6 | Activity MD/PA |
| Pneumatosis Intestinalis | Pneumatosis intestinalis can be classified as primary or secondary, but both are representative of underlying pathology. Pathophysiology and etiology ... Read the Article | 1 | 5 | Activity DO |
| Pneumatosis Intestinalis | Pneumatosis intestinalis can be classified as primary or secondary, but both are representative of underlying pathology. Pathophysiology and etiology ... Read the Article | 1 | 5 | Activity MD/PA |
| Pneumococcal Vaccine | The advent of pneumococcal vaccines has proven to be a significant advancement in the treatment and prevention of a widespread and sometimes deadly di ... Read the Article | 1 | 6 | Activity DO |
| Pneumococcal Vaccine | The advent of pneumococcal vaccines has proven to be a significant advancement in the treatment and prevention of a widespread and sometimes deadly di ... Read the Article | 1 | 6 | Activity MD/PA |
| Poikiloderma Congenitale | Congenital poikiloderma, also known as Rothmund-Thomson syndrome (RTS), is a rare genodermatosis with autosomal recessive inheritance. It is character ... Read the Article | 1 | 4 | Activity DO |
| Poikiloderma Congenitale | Congenital poikiloderma, also known as Rothmund-Thomson syndrome (RTS), is a rare genodermatosis with autosomal recessive inheritance. It is character ... Read the Article | 1 | 4 | Activity MD/PA |
| Polycystic Kidney Disease Of Childhood | There are two inherited varieties of polycystic kidney disease (PKD): autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive pol ... Read the Article | 1 | 7 | Activity DO |
| Polycystic Kidney Disease Of Childhood | There are two inherited varieties of polycystic kidney disease (PKD): autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive pol ... Read the Article | 1 | 7 | Activity MD/PA |
| Polydactyly | Polydactyly may indicate the presence of a very serious underlying disease or may present as an isolated finding. It may present in upper extremity or ... Read the Article | 1 | 5 | Activity DO |
| Polydactyly | Polydactyly may indicate the presence of a very serious underlying disease or may present as an isolated finding. It may present in upper extremity or ... Read the Article | 1 | 5 | Activity MD/PA |
| Posterior Urethral Valve | This article contains a synopsis of the anatomy, embryology, and classification of posterior urethral valves with a brief discussion of the theories a ... Read the Article | 1 | 6 | Activity DO |
| Posterior Urethral Valve | This article contains a synopsis of the anatomy, embryology, and classification of posterior urethral valves with a brief discussion of the theories a ... Read the Article | 1 | 6 | Activity MD/PA |
| Potter Syndrome | Potter syndrome is a fatal congenital disorder characterized by the changes in physical appearances of neonate due to oligohydramnios caused by renal ... Read the Article | 1.25 | 10 | Activity DO |
| Potter Syndrome | Potter syndrome is a fatal congenital disorder characterized by the changes in physical appearances of neonate due to oligohydramnios caused by renal ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Prader-Willi Syndrome | Prader Willi syndrome (PWS) is a rare and complex genetic disease. The condition has numerous implications on metabolic, endocrine, and neurologic sys ... Read the Article | 1.25 | 10 | Activity DO |
| Prader-Willi Syndrome | Prader Willi syndrome (PWS) is a rare and complex genetic disease. The condition has numerous implications on metabolic, endocrine, and neurologic sys ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Pregnancy | Globally, there are more than 200 million pregnancies each year. Of these pregnancies, more than 40% are unintended. Unintended does not imply unwante ... Read the Article | 1.75 | 22 | Activity DO |
| Pregnancy | Globally, there are more than 200 million pregnancies each year. Of these pregnancies, more than 40% are unintended. Unintended does not imply unwante ... Read the Article | 1.75 | 22 | Activity MD/PA |
| Pregnancy And Viral Hepatitis | The common cause of jaundice in pregnancy is acute viral hepatitis. Hepatitis could be caused by diseases distinctively associated with pregnancy and ... Read the Article | 1 | 6 | Activity DO |
| Pregnancy And Viral Hepatitis | The common cause of jaundice in pregnancy is acute viral hepatitis. Hepatitis could be caused by diseases distinctively associated with pregnancy and ... Read the Article | 1 | 6 | Activity MD/PA |
| Prenatal Non-stress Test | Prenatal non-stress test, popularly known as NST, is a method used to test fetal wellbeing before the onset of labor. A prenatal non-stress test funct ... Read the Article | 1.25 | 10 | Activity DO |
| Prenatal Non-stress Test | Prenatal non-stress test, popularly known as NST, is a method used to test fetal wellbeing before the onset of labor. A prenatal non-stress test funct ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Preterm Labor | Preterm labor is labor occurring between after 20 and before 37 weeks gestation. Preterm labors are subcategorized as early or late preterm. Early pre ... Read the Article | 1.25 | 13 | Activity DO |
| Preterm Labor | Preterm labor is labor occurring between after 20 and before 37 weeks gestation. Preterm labors are subcategorized as early or late preterm. Early pre ... Read the Article | 1.25 | 13 | Activity MD/PA |
| Prostaglandin E1 | Prostaglandin E1 (PGE1) is a medication used in the management of erectile dysfunction and ductus arteriosus in neonates. It is a smooth muscle relaxa ... Read the Article | 1 | 4 | Activity DO |
| Prostaglandin E1 | Prostaglandin E1 (PGE1) is a medication used in the management of erectile dysfunction and ductus arteriosus in neonates. It is a smooth muscle relaxa ... Read the Article | 1 | 4 | Activity MD/PA |
| Protein C Deficiency | Protein C deficiency is a rare but serious condition that can be congenital or acquired. Patients with this condition have a higher propensity to deve ... Read the Article | 1 | 5 | Activity DO |
| Protein C Deficiency | Protein C deficiency is a rare but serious condition that can be congenital or acquired. Patients with this condition have a higher propensity to deve ... Read the Article | 1 | 5 | Activity MD/PA |
| Prune Belly Syndrome | Prune belly syndrome is a rare congenitally acquired disorder primarily characterized by the clinical triad of deficient abdominal musculature, crypto ... Read the Article | 1.25 | 8 | Activity DO |
| Prune Belly Syndrome | Prune belly syndrome is a rare congenitally acquired disorder primarily characterized by the clinical triad of deficient abdominal musculature, crypto ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Pulmonary Artery Sling | Pulmonary artery sling is a specific type of anatomical vascular anomaly that can compress nearby structures. Instead of arising from the main pulmona ... Read the Article | 1 | 5 | Activity DO |
| Pulmonary Artery Sling | Pulmonary artery sling is a specific type of anatomical vascular anomaly that can compress nearby structures. Instead of arising from the main pulmona ... Read the Article | 1 | 5 | Activity MD/PA |
| Pulmonary Atresia With Intact Ventricular Septum | This activity provides a detailed review of the complex congenital heart defect pulmonary atresia with the intact ventricular septum. This review art ... Read the Article | 1 | 4 | Activity DO |
| Pulmonary Atresia With Intact Ventricular Septum | This activity provides a detailed review of the complex congenital heart defect pulmonary atresia with the intact ventricular septum. This review art ... Read the Article | 1 | 4 | Activity MD/PA |
| Pulmonary Atresia With Ventricular Septal Defect | Pulmonary atresia with ventricular septal defect is a rare congenital anomaly with poor prognostic outcomes. It is a serious anomaly affecting the dev ... Read the Article | 1 | 7 | Activity DO |
| Pulmonary Atresia With Ventricular Septal Defect | Pulmonary atresia with ventricular septal defect is a rare congenital anomaly with poor prognostic outcomes. It is a serious anomaly affecting the dev ... Read the Article | 1 | 7 | Activity MD/PA |
| Pulmonary Interstitial Emphysema | Pulmonary interstitial emphysema (PIE) is a rare disease that most commonly occurs in premature infants but can be seen in adults as well. Pathology i ... Read the Article | 1 | 5 | Activity DO |
| Pulmonary Interstitial Emphysema | Pulmonary interstitial emphysema (PIE) is a rare disease that most commonly occurs in premature infants but can be seen in adults as well. Pathology i ... Read the Article | 1 | 5 | Activity MD/PA |
| Pulmonary Sequestration | Pulmonary sequestration is thought to account for less than 6 percent of congenital lung malformations. In this condition, there is a nonfunctional se ... Read the Article | 1 | 5 | Activity DO |
| Pulmonary Sequestration | Pulmonary sequestration is thought to account for less than 6 percent of congenital lung malformations. In this condition, there is a nonfunctional se ... Read the Article | 1 | 5 | Activity MD/PA |
| Pyloric Stenosis | Pyloric stenosis, also known as infantile hypertrophic pyloric stenosis (IHPS), is an uncommon condition in infants characterized by abnormal thickeni ... Read the Article | 1.25 | 12 | Activity DO |
| Pyloric Stenosis | Pyloric stenosis, also known as infantile hypertrophic pyloric stenosis (IHPS), is an uncommon condition in infants characterized by abnormal thickeni ... Read the Article | 1.25 | 12 | Activity MD/PA |
| Renal Artery Thrombosis | Renal artery thrombosis is a rare pathology that may be overlooked when evaluating impaired renal function. It is the formation of a blood clot in one ... Read the Article | 1 | 5 | Activity DO |
| Renal Artery Thrombosis | Renal artery thrombosis is a rare pathology that may be overlooked when evaluating impaired renal function. It is the formation of a blood clot in one ... Read the Article | 1 | 5 | Activity MD/PA |
| Rh Incompatibility | Rhesus (Rh) incompatibility refers to the discordant pairing of maternal and fetal Rh type. It is associated with the development of maternal Rh sensi ... Read the Article | 1 | 5 | Activity DO |
| Rh Incompatibility | Rhesus (Rh) incompatibility refers to the discordant pairing of maternal and fetal Rh type. It is associated with the development of maternal Rh sensi ... Read the Article | 1 | 5 | Activity MD/PA |
| Rh-Hemolytic Disease | Rh-hemolytic disease develops due to the conception of an Rh-negative female with an Rh-positive fetus and can cause a broad range of symptoms in the ... Read the Article | 1 | 5 | Activity DO |
| Rh-Hemolytic Disease | Rh-hemolytic disease develops due to the conception of an Rh-negative female with an Rh-positive fetus and can cause a broad range of symptoms in the ... Read the Article | 1 | 5 | Activity MD/PA |
| Right Aortic Arches | Right aortic arch anomalies occur in approximately 0.01 to 0.1 percent of the general population. In general, these anomalies do not directly cause an ... Read the Article | 1.25 | 9 | Activity DO |
| Right Aortic Arches | Right aortic arch anomalies occur in approximately 0.01 to 0.1 percent of the general population. In general, these anomalies do not directly cause an ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Roseola Infantum | Roseola infantum is a common disease of childhood that is seen globally and is caused by infection with human herpesvirus 6 (HHV-6), or, less frequent ... Read the Article | 1.25 | 13 | Activity DO |
| Roseola Infantum | Roseola infantum is a common disease of childhood that is seen globally and is caused by infection with human herpesvirus 6 (HHV-6), or, less frequent ... Read the Article | 1.25 | 13 | Activity MD/PA |
| Rubella | Rubella is a mild viral disease that typically occurs in children and non-immune young adults. In pregnant women, rubella infection can produce a cons ... Read the Article | 1.25 | 10 | Activity DO |
| Rubella | Rubella is a mild viral disease that typically occurs in children and non-immune young adults. In pregnant women, rubella infection can produce a cons ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Scalp Catheterization | Peripheral venous access is a key need for resuscitating patients of all ages. An ideal site for venous catheterization is one that is easy to access ... Read the Article | 1 | 5 | Activity DO |
| Scalp Catheterization | Peripheral venous access is a key need for resuscitating patients of all ages. An ideal site for venous catheterization is one that is easy to access ... Read the Article | 1 | 5 | Activity MD/PA |
| Septic Hip Joint | Septic arthritis in the pediatric hip is an emergent surgical condition that if not rapidly treated, can lead to the rapid destruction of the hip, sep ... Read the Article | 1 | 8 | Activity DO |
| Septic Hip Joint | Septic arthritis in the pediatric hip is an emergent surgical condition that if not rapidly treated, can lead to the rapid destruction of the hip, sep ... Read the Article | 1 | 8 | Activity MD/PA |
| Shoulder Dystocia | Shoulder dystocia is a complication of vaginal delivery in which the baby's shoulder gets caught above the mother's pubic bone. It is characterized by ... Read the Article | 1.25 | 9 | Activity DO |
| Shoulder Dystocia | Shoulder dystocia is a complication of vaginal delivery in which the baby's shoulder gets caught above the mother's pubic bone. It is characterized by ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Sickle Cell Anemia | Sickle cell anemia is an inherited disorder of the globin chains that causes hemolysis and chronic organ damage. This activity reviews the pathophysio ... Read the Article | 2 | 21 | Activity DO |
| Sickle Cell Anemia | Sickle cell anemia is an inherited disorder of the globin chains that causes hemolysis and chronic organ damage. This activity reviews the pathophysio ... Read the Article | 2 | 21 | Activity MD/PA |
| Sickle Cell Trait | Sickle cell trait (SCT) is a benign condition in which the affected individual has only one abnormal hemoglobin beta gene allele. This is in contrast ... Read the Article | 1 | 6 | Activity DO |
| Sickle Cell Trait | Sickle cell trait (SCT) is a benign condition in which the affected individual has only one abnormal hemoglobin beta gene allele. This is in contrast ... Read the Article | 1 | 6 | Activity MD/PA |
| Small for Gestational Age | Small for gestational age (SGA) is defined as a birth weight of less than 10th percentile for gestational age. The burden of fetal growth-restricted ( ... Read the Article | 1 | 6 | Activity DO |
| Small for Gestational Age | Small for gestational age (SGA) is defined as a birth weight of less than 10th percentile for gestational age. The burden of fetal growth-restricted ( ... Read the Article | 1 | 6 | Activity MD/PA |
| Sonography Evaluation Of Amniotic Fluid | Amniotic fluid is produced and processed largely by the fetus. Two main methods are used to communicate amniotic fluid levels: the amniotic fluid ind ... Read the Article | 1 | 7 | Activity DO |
| Sonography Evaluation Of Amniotic Fluid | Amniotic fluid is produced and processed largely by the fetus. Two main methods are used to communicate amniotic fluid levels: the amniotic fluid ind ... Read the Article | 1 | 7 | Activity MD/PA |
| Spina Bifida | Spina Bifida is a generalized term for the neurologic condition resulting from the failure of neural tube closure of varying degrees during fetal deve ... Read the Article | 1.25 | 12 | Activity DO |
| Spina Bifida | Spina Bifida is a generalized term for the neurologic condition resulting from the failure of neural tube closure of varying degrees during fetal deve ... Read the Article | 1.25 | 12 | Activity MD/PA |
| Spinal Dysraphism And Myelomeningocele | Spinal dysraphism is a congenital abnormality that results in an abnormal structure in the spine, including the bony structure, the spinal cord, and t ... Read the Article | 1.25 | 10 | Activity DO |
| Spinal Dysraphism And Myelomeningocele | Spinal dysraphism is a congenital abnormality that results in an abnormal structure in the spine, including the bony structure, the spinal cord, and t ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Spinal Muscle Atrophy | Spinal muscular atrophy is an inherited autosomal recessive disease of a varying phenotype that is characterized by progressive muscle weakness, reduc ... Read the Article | 1.25 | 7 | Activity DO |
| Spinal Muscle Atrophy | Spinal muscular atrophy is an inherited autosomal recessive disease of a varying phenotype that is characterized by progressive muscle weakness, reduc ... Read the Article | 1.25 | 7 | Activity MD/PA |
| Streptococcal Meningitis | Streptococcal meningitis is an acute, purulent inflammation of the membranes surrounding the brain and spinal cord caused by bacteria from the Strepto ... Read the Article | 1 | 7 | Activity DO |
| Streptococcal Meningitis | Streptococcal meningitis is an acute, purulent inflammation of the membranes surrounding the brain and spinal cord caused by bacteria from the Strepto ... Read the Article | 1 | 7 | Activity MD/PA |
| Streptococcus Group B | Group B Streptococcus (GBS) commonly appears in up to 35% of healthy women's reproductive or gastrointestinal tracts. Pregnant women colonized with GB ... Read the Article | 1 | 5 | Activity DO |
| Streptococcus Group B | Group B Streptococcus (GBS) commonly appears in up to 35% of healthy women's reproductive or gastrointestinal tracts. Pregnant women colonized with GB ... Read the Article | 1 | 5 | Activity MD/PA |
| Sturge-Weber Syndrome | Sturge-Weber syndrome, also known as encephalotrigeminal angiomatosis, is a neurocutaneous disorder characterized by angiomas involving the face, chor ... Read the Article | 1.25 | 11 | Activity DO |
| Sturge-Weber Syndrome | Sturge-Weber syndrome, also known as encephalotrigeminal angiomatosis, is a neurocutaneous disorder characterized by angiomas involving the face, chor ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Subdural Hematoma | A subdural hematoma, as its name implies, forms because of an abnormal collection of blood under the dura mater. This is one of the intracranial injur ... Read the Article | 1.75 | 20 | Activity DO |
| Subdural Hematoma | A subdural hematoma, as its name implies, forms because of an abnormal collection of blood under the dura mater. This is one of the intracranial injur ... Read the Article | 1.75 | 20 | Activity MD/PA |
| Subglottic Stenosis | Subglottic stenosis can be defined as the narrowing of the upper airway, which lies between the vocal folds and the lower border of the cricoid cartil ... Read the Article | 1.25 | 8 | Activity DO |
| Subglottic Stenosis | Subglottic stenosis can be defined as the narrowing of the upper airway, which lies between the vocal folds and the lower border of the cricoid cartil ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Substance Use In Pregnancy | Substance use disorder (SUD) in pregnancy is a growing concern in the United States. Patients with substance use disorders in the peripartum period fa ... Read the Article | 1.25 | 6 | Activity DO |
| Substance Use In Pregnancy | Substance use disorder (SUD) in pregnancy is a growing concern in the United States. Patients with substance use disorders in the peripartum period fa ... Read the Article | 1.25 | 6 | Activity MD/PA |
| Sudden Infant Death Syndrome | Sudden infant death syndrome (SIDS) is the abrupt and unexplained death of an infant less than 1-year old. Despite a thorough investigation (a careful ... Read the Article | 1.25 | 9 | Activity DO |
| Sudden Infant Death Syndrome | Sudden infant death syndrome (SIDS) is the abrupt and unexplained death of an infant less than 1-year old. Despite a thorough investigation (a careful ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Suprapubic Aspiration | Suprapubic aspiration is a procedure performed to obtain a urine sample. It is often done when a urinary catheter cannot be placed. It is commonly per ... Read the Article | 1 | 5 | Activity DO |
| Suprapubic Aspiration | Suprapubic aspiration is a procedure performed to obtain a urine sample. It is often done when a urinary catheter cannot be placed. It is commonly per ... Read the Article | 1 | 5 | Activity MD/PA |
| Supravalvar Aortic Stenosis | Supravalvular aortic stenosis (SVAS) is a congenital heart defect that accounts for 8 to 14 percent of all cases of congenital aortic stenosis. It inv ... Read the Article | 1 | 4 | Activity DO |
| Supravalvar Aortic Stenosis | Supravalvular aortic stenosis (SVAS) is a congenital heart defect that accounts for 8 to 14 percent of all cases of congenital aortic stenosis. It inv ... Read the Article | 1 | 4 | Activity MD/PA |
| Surfactant | Pulmonary surfactant is a lipoprotein complex that lines the alveoli and decreases the surface tension to prevent lung atelectasis. Surfactant deficie ... Read the Article | 1.25 | 8 | Activity DO |
| Surfactant | Pulmonary surfactant is a lipoprotein complex that lines the alveoli and decreases the surface tension to prevent lung atelectasis. Surfactant deficie ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Tay-Sachs Disease | Tay Sachs disease is a rare autosomal recessive progressive neurodegenerative disorder. Patients usually exhibit a severe clinical course with death i ... Read the Article | 1.75 | 22 | Activity DO |
| Tay-Sachs Disease | Tay Sachs disease is a rare autosomal recessive progressive neurodegenerative disorder. Patients usually exhibit a severe clinical course with death i ... Read the Article | 1.75 | 22 | Activity MD/PA |
| Tetanus | Tetanus is an infection characterized by muscle spasms and lockjaw, also called trismus. Toxins produced by Clostridium tetani are responsible for the ... Read the Article | 1.5 | 17 | Activity DO |
| Tetanus | Tetanus is an infection characterized by muscle spasms and lockjaw, also called trismus. Toxins produced by Clostridium tetani are responsible for the ... Read the Article | 1.5 | 17 | Activity MD/PA |
| Tetracycline | Tetracyclines (tetracycline, doxycycline, minocycline, tigecycline) are a class of medication used to manage and treat various bacterial infections. T ... Read the Article | 1 | 5 | Activity DO |
| Tetracycline | Tetracyclines (tetracycline, doxycycline, minocycline, tigecycline) are a class of medication used to manage and treat various bacterial infections. T ... Read the Article | 1 | 5 | Activity MD/PA |
| Thrombocytopenia in Pregnancy | Thrombocytopenia, defined as a platelet count of under 150 x 10^9/L, is the second most common hematological abnormality in pregnancy. This CME activi ... Read the Article | 1.25 | 7 | Activity DO |
| Thrombocytopenia in Pregnancy | Thrombocytopenia, defined as a platelet count of under 150 x 10^9/L, is the second most common hematological abnormality in pregnancy. This CME activi ... Read the Article | 1.25 | 7 | Activity MD/PA |
| TORCH Complex | The term TORCH complex or TORCHes infection includes toxoplasmosis, others (syphilis, hepatitis B), rubella, cytomegalovirus, herpes simplex. These ar ... Read the Article | 1 | 5 | Activity DO |
| TORCH Complex | The term TORCH complex or TORCHes infection includes toxoplasmosis, others (syphilis, hepatitis B), rubella, cytomegalovirus, herpes simplex. These ar ... Read the Article | 1 | 5 | Activity MD/PA |
| Toxoplasma Retinochoroiditis | Toxoplasma retinochoroiditis (TRC) is likely the most common cause of infectious retinochoroiditis worldwide. One-quarter of patients with a history o ... Read the Article | 1 | 7 | Activity DO |
| Toxoplasma Retinochoroiditis | Toxoplasma retinochoroiditis (TRC) is likely the most common cause of infectious retinochoroiditis worldwide. One-quarter of patients with a history o ... Read the Article | 1 | 7 | Activity MD/PA |
| Tracheoesophageal Fistula | Tracheoesophageal fistulas (TEFs) represent one of the most common congenital anomalies seen in major pediatric surgical centers. Infants with tracheo ... Read the Article | 1.25 | 8 | Activity DO |
| Tracheoesophageal Fistula | Tracheoesophageal fistulas (TEFs) represent one of the most common congenital anomalies seen in major pediatric surgical centers. Infants with tracheo ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Tracheomalacia | Tracheomalacia is a condition that is characterized by excessive collapsibility of the trachea. Depending on the severity of the disease, patients’ sy ... Read the Article | 1 | 5 | Activity DO |
| Tracheomalacia | Tracheomalacia is a condition that is characterized by excessive collapsibility of the trachea. Depending on the severity of the disease, patients’ sy ... Read the Article | 1 | 5 | Activity MD/PA |
| Transient Tachypnea of the Newborn | Transient tachypnea of the newborn (TTN) is a benign, self-limited condition that can present in infants of any gestational age shortly after birth. I ... Read the Article | 1.25 | 9 | Activity DO |
| Transient Tachypnea of the Newborn | Transient tachypnea of the newborn (TTN) is a benign, self-limited condition that can present in infants of any gestational age shortly after birth. I ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Transposition Of The Great Arteries | Transposition of the great arteries (TGA) is a congenital pediatric cardiac defect arising from an embryological discordance between the aorta and pul ... Read the Article | 1.25 | 12 | Activity DO |
| Transposition Of The Great Arteries | Transposition of the great arteries (TGA) is a congenital pediatric cardiac defect arising from an embryological discordance between the aorta and pul ... Read the Article | 1.25 | 12 | Activity MD/PA |
| Trichomoniasis | Trichomonas vaginalis is a protozoan responsible for trichomoniasis, one of the most prevalent non-viral sexually transmitted infections (STIs) in the ... Read the Article | 1.5 | 19 | Activity DO |
| Trichomoniasis | Trichomonas vaginalis is a protozoan responsible for trichomoniasis, one of the most prevalent non-viral sexually transmitted infections (STIs) in the ... Read the Article | 1.5 | 19 | Activity MD/PA |
| Tricuspid Atresia | Tricuspid atresia is a cyanotic congenital heart defect characterized by the complete agenesis of the tricuspid valve. This activity reviews the evalu ... Read the Article | 1.5 | 13 | Activity DO |
| Tricuspid Atresia | Tricuspid atresia is a cyanotic congenital heart defect characterized by the complete agenesis of the tricuspid valve. This activity reviews the evalu ... Read the Article | 1.5 | 13 | Activity MD/PA |
| Tricuspid Regurgitation | Tricuspid regurgitation, also called tricuspid insufficiency, is a relatively common condition that can result from structural abnormalities of any pa ... Read the Article | 1 | 7 | Activity DO |
| Tricuspid Regurgitation | Tricuspid regurgitation, also called tricuspid insufficiency, is a relatively common condition that can result from structural abnormalities of any pa ... Read the Article | 1 | 7 | Activity MD/PA |
| Trisomy 13 | Trisomy 13 is a chromosomal aneuploidy characterized by meiotic nondisjunction. The phenotypic holoprosencephaly and midline fusion aberrancies are re ... Read the Article | 1 | 6 | Activity DO |
| Trisomy 13 | Trisomy 13 is a chromosomal aneuploidy characterized by meiotic nondisjunction. The phenotypic holoprosencephaly and midline fusion aberrancies are re ... Read the Article | 1 | 6 | Activity MD/PA |
| Truncus Arteriosus | Persistent truncus arteriosus (TA) is a rare, congenital, cyanotic heart defect characterized by a ventricular septal defect (VSD), a single truncal v ... Read the Article | 1.25 | 9 | Activity DO |
| Truncus Arteriosus | Persistent truncus arteriosus (TA) is a rare, congenital, cyanotic heart defect characterized by a ventricular septal defect (VSD), a single truncal v ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Turner Syndrome | Turner syndrome, also referred to as congenital ovarian hypoplasia syndrome is the most common sex chromosomal abnormality found in females. It result ... Read the Article | 1.5 | 19 | Activity DO |
| Turner Syndrome | Turner syndrome, also referred to as congenital ovarian hypoplasia syndrome is the most common sex chromosomal abnormality found in females. It result ... Read the Article | 1.5 | 19 | Activity MD/PA |
| Umbilical Artery Catheterization | Catheterization of an umbilical artery is one of the commonly performed procedures in extremely premature neonates. This activity reviews the indicati ... Read the Article | 1 | 6 | Activity DO |
| Umbilical Artery Catheterization | Catheterization of an umbilical artery is one of the commonly performed procedures in extremely premature neonates. This activity reviews the indicati ... Read the Article | 1 | 6 | Activity MD/PA |
| Umbilical Hernia | An umbilical hernia is a ventral hernia located at or near the umbilicus. In general, umbilical hernias tend to have a narrow neck, which increases ... Read the Article | 1.25 | 8 | Activity DO |
| Umbilical Hernia | An umbilical hernia is a ventral hernia located at or near the umbilicus. In general, umbilical hernias tend to have a narrow neck, which increases ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Umbilical Vein Catheterization | Umbilical vein catheterization utilizes the exposed umbilical stump in a neonate as a site for emergency central venous access up to 14 days old. Umbi ... Read the Article | 1.25 | 9 | Activity DO |
| Umbilical Vein Catheterization | Umbilical vein catheterization utilizes the exposed umbilical stump in a neonate as a site for emergency central venous access up to 14 days old. Umbi ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Unconjugated Hyperbilirubinemia | Unconjugated hyperbilirubinemia is a condition defined as elevated serum or plasma bilirubin (unconjugated) levels above the reference range of the la ... Read the Article | 1.25 | 10 | Activity DO |
| Unconjugated Hyperbilirubinemia | Unconjugated hyperbilirubinemia is a condition defined as elevated serum or plasma bilirubin (unconjugated) levels above the reference range of the la ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Understanding and Application of CDC Immunization Guidelines | Immunization is the most effective and safe public health intervention in reducing the incidence, prevalence, morbidity, and mortality of various infe ... Read the Article | 1.25 | 9 | Activity DO |
| Understanding and Application of CDC Immunization Guidelines | Immunization is the most effective and safe public health intervention in reducing the incidence, prevalence, morbidity, and mortality of various infe ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Upper Airway Resistance Syndrome | Upper airway resistance syndrome, commonly known as UARS, is a disorder included with many others that encompass an umbrella of conditions characteriz ... Read the Article | 1 | 6 | Activity DO |
| Upper Airway Resistance Syndrome | Upper airway resistance syndrome, commonly known as UARS, is a disorder included with many others that encompass an umbrella of conditions characteriz ... Read the Article | 1 | 6 | Activity MD/PA |
| Urea Cycle Disorders | Urea cycle disorders are inborn errors of metabolism resulting from defects in one of the enzymes or transporter molecules involved in the hepatic rem ... Read the Article | 1.25 | 8 | Activity DO |
| Urea Cycle Disorders | Urea cycle disorders are inborn errors of metabolism resulting from defects in one of the enzymes or transporter molecules involved in the hepatic rem ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Ureteropelvic Junction Obstruction | Ureteropelvic junction obstruction (UPJO) is one of the most common causes of hydronephrosis in children. If it is left untreated, it might cause loss ... Read the Article | 1 | 5 | Activity DO |
| Ureteropelvic Junction Obstruction | Ureteropelvic junction obstruction (UPJO) is one of the most common causes of hydronephrosis in children. If it is left untreated, it might cause loss ... Read the Article | 1 | 5 | Activity MD/PA |
| Vagal Maneuver | Vagal maneuvers are techniques used to increase vagal parasympathetic tone in an attempt to diagnose and treat various arrhythmias. They are often uti ... Read the Article | 1 | 5 | Activity DO |
| Vagal Maneuver | Vagal maneuvers are techniques used to increase vagal parasympathetic tone in an attempt to diagnose and treat various arrhythmias. They are often uti ... Read the Article | 1 | 5 | Activity MD/PA |
| Varicella Zoster | Chickenpox or varicella is a contagious disease caused by the varicella-zoster virus (VZV). The virus is responsible for chickenpox (usually primary i ... Read the Article | 2 | 27 | Activity DO |
| Varicella Zoster | Chickenpox or varicella is a contagious disease caused by the varicella-zoster virus (VZV). The virus is responsible for chickenpox (usually primary i ... Read the Article | 2 | 27 | Activity MD/PA |
| Varicella Zoster Immune Globulin | Varicella-zoster immune globulin (VZIG) is a medication used for postexposure prophylaxis and treatment of varicella. It is in the "Opportunistic Infe ... Read the Article | 1 | 5 | Activity DO |
| Varicella Zoster Immune Globulin | Varicella-zoster immune globulin (VZIG) is a medication used for postexposure prophylaxis and treatment of varicella. It is in the "Opportunistic Infe ... Read the Article | 1 | 5 | Activity MD/PA |
| Vascular Ring Double Aortic Arch | The term "vascular ring" refers to the vascular structures that encircle and compress the trachea and esophagus, causing respiratory and gastrointesti ... Read the Article | 1 | 7 | Activity DO |
| Vascular Ring Double Aortic Arch | The term "vascular ring" refers to the vascular structures that encircle and compress the trachea and esophagus, causing respiratory and gastrointesti ... Read the Article | 1 | 7 | Activity MD/PA |
| Venezuelan Equine Encephalitis | Venezuelan equine encephalitis (VEE) is a mosquito-borne disease endemic in regions of Central and South America that causes sporadic outbreaks of equ ... Read the Article | 1 | 6 | Activity DO |
| Venezuelan Equine Encephalitis | Venezuelan equine encephalitis (VEE) is a mosquito-borne disease endemic in regions of Central and South America that causes sporadic outbreaks of equ ... Read the Article | 1 | 6 | Activity MD/PA |
| Ventricular Septal Defect | Ventricular septal defects (VSDs) are the most common congenital cardiac anomaly in children and the second most common congenital abnormality in adul ... Read the Article | 1.5 | 14 | Activity DO |
| Ventricular Septal Defect | Ventricular septal defects (VSDs) are the most common congenital cardiac anomaly in children and the second most common congenital abnormality in adul ... Read the Article | 1.5 | 14 | Activity MD/PA |
| Ventriculitis | Ventriculitis is the inflammation of the ependymal lining of the cerebral ventricles, usually secondary to infection (for example meningitis, device-r ... Read the Article | 1 | 6 | Activity DO |
| Ventriculitis | Ventriculitis is the inflammation of the ependymal lining of the cerebral ventricles, usually secondary to infection (for example meningitis, device-r ... Read the Article | 1 | 6 | Activity MD/PA |
| Viral Myocarditis | Myocarditis is an inflammatory process of the myocardium. It can present in the acute, subacute, or chronic phase with either focal or diffuse involve ... Read the Article | 1.25 | 11 | Activity DO |
| Viral Myocarditis | Myocarditis is an inflammatory process of the myocardium. It can present in the acute, subacute, or chronic phase with either focal or diffuse involve ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Viral Pneumonia | The increasing role of viral pathogens in pneumonia and the increased recognition of bacterial and viral coinfections in patients with pneumonia neces ... Read the Article | 1.25 | 7 | Activity DO |
| Viral Pneumonia | The increasing role of viral pathogens in pneumonia and the increased recognition of bacterial and viral coinfections in patients with pneumonia neces ... Read the Article | 1.25 | 7 | Activity MD/PA |
| Vitamin A Toxicity | Vitamin A toxicity can due to either topical or oral vitamin A administration. Oral vitamin A toxicity can be acute, due to the ingestion of a large a ... Read the Article | 1 | 6 | Activity DO |
| Vitamin A Toxicity | Vitamin A toxicity can due to either topical or oral vitamin A administration. Oral vitamin A toxicity can be acute, due to the ingestion of a large a ... Read the Article | 1 | 6 | Activity MD/PA |
| Vitamin B6 Deficiency | Water-soluble vitamin B6 is widely present in many foods, including meat, fish, nuts, beans, grains, fruits and vegetables. As a coenzyme, vitamin B6 ... Read the Article | 1 | 5 | Activity DO |
| Vitamin B6 Deficiency | Water-soluble vitamin B6 is widely present in many foods, including meat, fish, nuts, beans, grains, fruits and vegetables. As a coenzyme, vitamin B6 ... Read the Article | 1 | 5 | Activity MD/PA |
| Vitamin K Deficiency | Vitamin K refers to a group of fat-soluble compounds involved in coagulation, bone development, and cardiovascular health. Vitamin K deficiency can co ... Read the Article | 1.25 | 13 | Activity DO |
| Vitamin K Deficiency | Vitamin K refers to a group of fat-soluble compounds involved in coagulation, bone development, and cardiovascular health. Vitamin K deficiency can co ... Read the Article | 1.25 | 13 | Activity MD/PA |
| Waardenburg Syndrome | Waardenburg syndrome is a group of genetic conditions inherited in an autosomal dominant fashion. During embryogenesis, there is an abnormal distribut ... Read the Article | 1 | 6 | Activity DO |
| Waardenburg Syndrome | Waardenburg syndrome is a group of genetic conditions inherited in an autosomal dominant fashion. During embryogenesis, there is an abnormal distribut ... Read the Article | 1 | 6 | Activity MD/PA |
| Werdnig Hoffmann Disease | Werdnig-Hoffmann disease is a type of spinal muscular atrophy (SMA). It is the most common type of SMA and accounts for about 80% of individuals with ... Read the Article | 1 | 5 | Activity DO |
| Werdnig Hoffmann Disease | Werdnig-Hoffmann disease is a type of spinal muscular atrophy (SMA). It is the most common type of SMA and accounts for about 80% of individuals with ... Read the Article | 1 | 5 | Activity MD/PA |
| Williams Syndrome | Williams syndrome is a rare genetic disorder with congenital heart disease, distinctive facial features (elfin-like faces), hypercalcemia, neurodevelo ... Read the Article | 1 | 6 | Activity DO |
| Williams Syndrome | Williams syndrome is a rare genetic disorder with congenital heart disease, distinctive facial features (elfin-like faces), hypercalcemia, neurodevelo ... Read the Article | 1 | 6 | Activity MD/PA |
| Zellweger Syndrome | Zellweger syndrome, also known as cerebrohepatorenal syndrome, is a rare inherited disorder characterized by the absence or reduction of functional pe ... Read the Article | 1 | 5 | Activity DO |
| Zellweger Syndrome | Zellweger syndrome, also known as cerebrohepatorenal syndrome, is a rare inherited disorder characterized by the absence or reduction of functional pe ... Read the Article | 1 | 5 | Activity MD/PA |
| Zika Virus | Zika virus is a single-stranded RNA virus of the family and the genus Flavivirus. In the majority of people, infection by the Zika virus is mild and s ... Read the Article | 1.25 | 10 | Activity DO |
| Zika Virus | Zika virus is a single-stranded RNA virus of the family and the genus Flavivirus. In the majority of people, infection by the Zika virus is mild and s ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Zinc Deficiency | Zinc deficiency is common worldwide but is seen with greater frequency in developing countries. Zinc deficiency can be inherited or acquired and typic ... Read the Article | 1 | 7 | Activity DO |
| Zinc Deficiency | Zinc deficiency is common worldwide but is seen with greater frequency in developing countries. Zinc deficiency can be inherited or acquired and typic ... Read the Article | 1 | 7 | Activity MD/PA |
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