Pathology-Pediatric CME
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Pathology-Pediatric Articles (342)
Featured Activities
Pathology-Pediatric 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 | 5 | 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 | 5 | Activity MD/PA |
| Abetalipoproteinemia | Abetalipoproteinemia is a rare autosomal recessive disorder marked by low or absent levels of plasma cholesterol, low-density lipoproteins and very-lo ... Read the Article | 1.25 | 8 | Activity DO |
| Abetalipoproteinemia | Abetalipoproteinemia is a rare autosomal recessive disorder marked by low or absent levels of plasma cholesterol, low-density lipoproteins and very-lo ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Acquired Digital Fibrokeratoma | Acquired digital fibrokeratoma (ADFK) is a rare, benign, fibrous tumor. It usually occurs in adults as a solitary lesion on fingers and toes. Since AD ... Read the Article | 1 | 6 | Activity DO |
| Acquired Digital Fibrokeratoma | Acquired digital fibrokeratoma (ADFK) is a rare, benign, fibrous tumor. It usually occurs in adults as a solitary lesion on fingers and toes. Since AD ... Read the Article | 1 | 6 | 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 |
| Acrodynia | Acrodynia is a rare disorder caused due to chronic mercury poisoning or idiosyncrasy to mercury. It is a Greek term that means 'painful extremities.' ... Read the Article | 1 | 5 | Activity DO |
| Acrodynia | Acrodynia is a rare disorder caused due to chronic mercury poisoning or idiosyncrasy to mercury. It is a Greek term that means 'painful extremities.' ... Read the Article | 1 | 5 | Activity MD/PA |
| Acute Lymphocytic Leukemia | Acute lymphocytic leukemia (ALL) is a malignancy of B or T lymphoblasts characterized by uncontrolled proliferation of abnormal, immature lymphocytes ... Read the Article | 1.25 | 10 | Activity DO |
| Acute Lymphocytic Leukemia | Acute lymphocytic leukemia (ALL) is a malignancy of B or T lymphoblasts characterized by uncontrolled proliferation of abnormal, immature lymphocytes ... Read the Article | 1.25 | 10 | 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 |
| Acute Myocarditis | Acute myocarditis is inflammation of the myocardium. It is typically seen in infants and teenagers but can occur at any age. It most commonly results ... Read the Article | 1 | 5 | Activity DO |
| Acute Myocarditis | Acute myocarditis is inflammation of the myocardium. It is typically seen in infants and teenagers but can occur at any age. It most commonly results ... Read the Article | 1 | 5 | Activity MD/PA |
| Acute Renal Tubular Necrosis | The most common intrinsic cause of acute kidney injury is acute tubular necrosis. Acute tubular necrosis is most common in hospitalized patients and c ... Read the Article | 1 | 7 | Activity DO |
| Acute Renal Tubular Necrosis | The most common intrinsic cause of acute kidney injury is acute tubular necrosis. Acute tubular necrosis is most common in hospitalized patients and c ... Read the Article | 1 | 7 | Activity MD/PA |
| Adenoiditis | Adenoiditis occurs when there is inflammation of the adenoid tissue resulting from infection, allergies, or irritation from stomach acid. Adenoiditis ... Read the Article | 1 | 5 | Activity DO |
| Adenoiditis | Adenoiditis occurs when there is inflammation of the adenoid tissue resulting from infection, allergies, or irritation from stomach acid. Adenoiditis ... Read the Article | 1 | 5 | 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 |
| Albright Hereditary Osteodystrophy | Albright hereditary osteodystrophy (AHO) is a hereditary condition due to inactivating GNAS1 gene mutation. AHO is characterized by a round face, shor ... Read the Article | 1 | 5 | Activity DO |
| Albright Hereditary Osteodystrophy | Albright hereditary osteodystrophy (AHO) is a hereditary condition due to inactivating GNAS1 gene mutation. AHO is characterized by a round face, shor ... Read the Article | 1 | 5 | Activity MD/PA |
| Alpers-Huttenlocher Syndrome | Alpers-Huttenlocher syndrome (AHS) is a rare disease that is important to consider in children presenting with neurologic and hepatic symptoms. This a ... Read the Article | 1 | 5 | Activity DO |
| Alpers-Huttenlocher Syndrome | Alpers-Huttenlocher syndrome (AHS) is a rare disease that is important to consider in children presenting with neurologic and hepatic symptoms. This a ... 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 |
| Amegakaryocytic Thrombocytopenia | Amegakaryocytic thrombocytopenia is a severe form of thrombocytopenia with reduced or absent megakaryocytes in the bone marrow. It can be congenital o ... Read the Article | 1 | 5 | Activity DO |
| Amegakaryocytic Thrombocytopenia | Amegakaryocytic thrombocytopenia is a severe form of thrombocytopenia with reduced or absent megakaryocytes in the bone marrow. It can be congenital o ... Read the Article | 1 | 5 | Activity MD/PA |
| Anaphylaxis | Anaphylaxis is an acute, life-threatening hypersensitivity disorder, defined as a generalized, rapidly evolving, multi-systemic allergic reaction. Ana ... Read the Article | 1.75 | 24 | Activity DO |
| Anaphylaxis | Anaphylaxis is an acute, life-threatening hypersensitivity disorder, defined as a generalized, rapidly evolving, multi-systemic allergic reaction. Ana ... Read the Article | 1.75 | 24 | Activity MD/PA |
| Androgen Insensitivity Syndrome | Androgen insensitivity syndrome (AIS) is a common etiology of sexual developmental disorders and results in varying phenotypes. These disorders of and ... Read the Article | 1 | 5 | Activity DO |
| Androgen Insensitivity Syndrome | Androgen insensitivity syndrome (AIS) is a common etiology of sexual developmental disorders and results in varying phenotypes. These disorders of and ... Read the Article | 1 | 5 | Activity MD/PA |
| Angiokeratoma Circumscriptum | Angiokeratomas are a group of capillary malformations characterized by vascular ectasias of the papillary dermis associated with hyperkeratosis, papil ... Read the Article | 1 | 5 | Activity DO |
| Angiokeratoma Circumscriptum | Angiokeratomas are a group of capillary malformations characterized by vascular ectasias of the papillary dermis associated with hyperkeratosis, papil ... Read the Article | 1 | 5 | 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 |
| Apert Syndrome | Apert syndrome is an autosomal dominant inherited craniosynostosis syndrome. Males and females are equally affected. The incidence of the disease sign ... Read the Article | 1 | 5 | Activity DO |
| Apert Syndrome | Apert syndrome is an autosomal dominant inherited craniosynostosis syndrome. Males and females are equally affected. The incidence of the disease sign ... Read the Article | 1 | 5 | Activity MD/PA |
| Arginase Deficiency | Argininemia is an autosomal recessive disorder causing hyperammonemia secondary to arginine accumulation. It is a disorder first noticed in children w ... Read the Article | 1 | 6 | Activity DO |
| Arginase Deficiency | Argininemia is an autosomal recessive disorder causing hyperammonemia secondary to arginine accumulation. It is a disorder first noticed in children w ... Read the Article | 1 | 6 | Activity MD/PA |
| Arteriovenous Malformation Of The Brain | Arteriovenous malformations (AVMs) are a developmental anomaly of the vascular system, consisting of tangles of poorly formed blood vessels in which t ... Read the Article | 1.25 | 10 | Activity DO |
| Arteriovenous Malformation Of The Brain | Arteriovenous malformations (AVMs) are a developmental anomaly of the vascular system, consisting of tangles of poorly formed blood vessels in which t ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Astrocytoma | Astrocytoma originates in astrocytes, which are a kind of glial cells in the cerebrum which are star-shaped. It is the most common glioma, usually aff ... Read the Article | 1.25 | 8 | Activity DO |
| Astrocytoma | Astrocytoma originates in astrocytes, which are a kind of glial cells in the cerebrum which are star-shaped. It is the most common glioma, usually aff ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Ataxia Telangiectasia | Ataxia telangiectasia (Louis-Bar Syndrome) is a rare autosomal recessive condition characterized by cutaneous telangiectasias, cerebellar atrophy with ... Read the Article | 1.25 | 13 | Activity DO |
| Ataxia Telangiectasia | Ataxia telangiectasia (Louis-Bar Syndrome) is a rare autosomal recessive condition characterized by cutaneous telangiectasias, cerebellar atrophy with ... Read the Article | 1.25 | 13 | Activity MD/PA |
| Atrial Myxoma | Myxomas are the most common primary cardiac tumor. It is estimated that more than 75% of myxomas originate in the left atrium either at the mitral ann ... Read the Article | 1.5 | 14 | Activity DO |
| Atrial Myxoma | Myxomas are the most common primary cardiac tumor. It is estimated that more than 75% of myxomas originate in the left atrium either at the mitral ann ... Read the Article | 1.5 | 14 | 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 Canal Defects | Atrioventricular canal defects comprise a spectrum of defects such as exclusive ventricular or atrial defects, septal defects, atrioventricular anomal ... Read the Article | 1 | 7 | Activity DO |
| Atrioventricular Canal Defects | Atrioventricular canal defects comprise a spectrum of defects such as exclusive ventricular or atrial defects, septal defects, atrioventricular anomal ... Read the Article | 1 | 7 | Activity MD/PA |
| Axenfeld-Rieger Syndrome | Axenfeld-Rieger syndrome (ARS) was previously known as Axenfeld anomaly; the latter term was used to describe one of three subvariants of this spectru ... Read the Article | 1 | 3 | Activity DO |
| Axenfeld-Rieger Syndrome | Axenfeld-Rieger syndrome (ARS) was previously known as Axenfeld anomaly; the latter term was used to describe one of three subvariants of this spectru ... Read the Article | 1 | 3 | Activity MD/PA |
| Bacterial Meningitis | Bacterial meningitis is an infection of the meninges that results in inflammation. It is a serious and life-threatening condition that requires prompt ... Read the Article | 1.5 | 18 | Activity DO |
| Bacterial Meningitis | Bacterial meningitis is an infection of the meninges that results in inflammation. It is a serious and life-threatening condition that requires prompt ... Read the Article | 1.5 | 18 | Activity MD/PA |
| Balanitis Xerotica Obliterans | Balanitis xerotica obliterans, also known as lichen sclerosus, are white inflammatory patches that can affect both males and females. In males, the af ... Read the Article | 1 | 5 | Activity DO |
| Balanitis Xerotica Obliterans | Balanitis xerotica obliterans, also known as lichen sclerosus, are white inflammatory patches that can affect both males and females. In males, the af ... Read the Article | 1 | 5 | Activity MD/PA |
| Becker Muscular Dystrophy | Becker muscular dystrophy (BMD) is an X-linked recessive disorder due to mutation in the dystrophin gene that results in progressive muscle degenerati ... Read the Article | 1 | 6 | Activity DO |
| Becker Muscular Dystrophy | Becker muscular dystrophy (BMD) is an X-linked recessive disorder due to mutation in the dystrophin gene that results in progressive muscle degenerati ... Read the Article | 1 | 6 | 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 |
| 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 | 1.25 | 7 | 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 | 1.25 | 7 | 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 |
| Blepharochalasis Syndrome | Blepharochalasis syndrome is a rare disease of unknown etiology. It is characterized by an active stage of recurrent episodes of upper lid swelling, f ... Read the Article | 1 | 5 | Activity DO |
| Blepharochalasis Syndrome | Blepharochalasis syndrome is a rare disease of unknown etiology. It is characterized by an active stage of recurrent episodes of upper lid swelling, f ... Read the Article | 1 | 5 | Activity MD/PA |
| Blue Nevus | Blue nevi are melanotic dermal lesions that commonly presents as a blue nodule on the scalp, extremities, sacrococcygeal region, or buttocks. Its char ... Read the Article | 1.25 | 8 | Activity DO |
| Blue Nevus | Blue nevi are melanotic dermal lesions that commonly presents as a blue nodule on the scalp, extremities, sacrococcygeal region, or buttocks. Its char ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Blue Rubber Bleb Nevus Syndrome | Blue rubber bleb nevus syndrome is also known as Bean syndrome. It is a rare syndrome of venous malformations that arise in the skin and gastrointesti ... Read the Article | 1 | 5 | Activity DO |
| Blue Rubber Bleb Nevus Syndrome | Blue rubber bleb nevus syndrome is also known as Bean syndrome. It is a rare syndrome of venous malformations that arise in the skin and gastrointesti ... Read the Article | 1 | 5 | Activity MD/PA |
| Bone Cyst | A simple bone cyst is a solitary, benign, fluid-filled, cyst that may be a single chamber or septated. The most common sites are the proximal humerus ... Read the Article | 1 | 5 | Activity DO |
| Bone Cyst | A simple bone cyst is a solitary, benign, fluid-filled, cyst that may be a single chamber or septated. The most common sites are the proximal humerus ... Read the Article | 1 | 5 | Activity MD/PA |
| Boutonneuse Fever | Boutonneuse fever is a disease caused by the rickettsia genus and is of the spotted fever group classification. This disease classically causes fever, ... Read the Article | 1 | 5 | Activity DO |
| Boutonneuse Fever | Boutonneuse fever is a disease caused by the rickettsia genus and is of the spotted fever group classification. This disease classically causes fever, ... 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 |
| 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 |
| Bruton Agammaglobulinemia | Bruton agammaglobulinemia, also known as X-linked agammaglobulinemia (XLA) or Bruton's agammaglobulinemia, is an inherited immunodeficiency disorder. ... Read the Article | 1 | 5 | Activity DO |
| Bruton Agammaglobulinemia | Bruton agammaglobulinemia, also known as X-linked agammaglobulinemia (XLA) or Bruton's agammaglobulinemia, is an inherited immunodeficiency disorder. ... Read the Article | 1 | 5 | Activity MD/PA |
| Bulimia Nervosa | Bulimia nervosa is a disorder that is characterized by binge eating and inappropriate compensatory behavior to control weight with potentially dangero ... Read the Article | 1.75 | 20 | Activity DO |
| Bulimia Nervosa | Bulimia nervosa is a disorder that is characterized by binge eating and inappropriate compensatory behavior to control weight with potentially dangero ... Read the Article | 1.75 | 20 | 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 |
| Capillary Infantile Hemangiomas | Capillary hemangiomas (infantile hemangiomas, juvenile hemangiomas, hemangioblastomas, or strawberry nevi of infancy) are common benign orbital neopla ... Read the Article | 1 | 7 | Activity DO |
| Capillary Infantile Hemangiomas | Capillary hemangiomas (infantile hemangiomas, juvenile hemangiomas, hemangioblastomas, or strawberry nevi of infancy) are common benign orbital neopla ... Read the Article | 1 | 7 | Activity MD/PA |
| Cardiac Fibroma | Cardiac fibromas are the second most common primary cardiac tumor after rhabdomyoma in children. They are primarily composed of connective tissue and ... Read the Article | 1 | 5 | Activity DO |
| Cardiac Fibroma | Cardiac fibromas are the second most common primary cardiac tumor after rhabdomyoma in children. They are primarily composed of connective tissue and ... Read the Article | 1 | 5 | 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 |
| Carotenemia | First described in 1919 by Hess and Meyers, carotenemia is the medical terminology describing yellow-orange skin pigmentation due to high levels of ca ... Read the Article | 1 | 8 | Activity DO |
| Carotenemia | First described in 1919 by Hess and Meyers, carotenemia is the medical terminology describing yellow-orange skin pigmentation due to high levels of ca ... Read the Article | 1 | 8 | 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 |
| 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 |
| Charcot Marie Tooth | Charcot-Marie-Tooth disease (CMT) is the commonest inherited neuromuscular disorder. It affects the peripheral nerves and leads to progressive weaknes ... Read the Article | 1.75 | 19 | Activity DO |
| Charcot Marie Tooth | Charcot-Marie-Tooth disease (CMT) is the commonest inherited neuromuscular disorder. It affects the peripheral nerves and leads to progressive weaknes ... Read the Article | 1.75 | 19 | 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 |
| Chediak Higashi Syndrome | Chediak Higashi syndrome (CHS) is an autosomal recessive disorder that is characterized by easy bruising, oculocutaneous albinism and recurrent pyogen ... Read the Article | 1 | 5 | Activity DO |
| Chediak Higashi Syndrome | Chediak Higashi syndrome (CHS) is an autosomal recessive disorder that is characterized by easy bruising, oculocutaneous albinism and recurrent pyogen ... Read the Article | 1 | 5 | Activity MD/PA |
| Childhood Brain Tumors | Pediatric brain tumors are the most common type of solid childhood cancer and only second to leukemia as a cause of pediatric malignancies. They are c ... Read the Article | 1.25 | 9 | Activity DO |
| Childhood Brain Tumors | Pediatric brain tumors are the most common type of solid childhood cancer and only second to leukemia as a cause of pediatric malignancies. They are c ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Chloramphenicol | Chloramphenicol is a medication used in the management and treatment of superficial eye infections such as bacterial conjunctivitis, and otitis extern ... Read the Article | 1 | 6 | Activity DO |
| Chloramphenicol | Chloramphenicol is a medication used in the management and treatment of superficial eye infections such as bacterial conjunctivitis, and otitis extern ... Read the Article | 1 | 6 | Activity MD/PA |
| Cholestatic Jaundice | Cholestasis is defined as stagnation, or at least a marked reduction, in bile secretion and flow. Cholestasis can be due to a functional impairment of ... Read the Article | 1 | 6 | Activity DO |
| Cholestatic Jaundice | Cholestasis is defined as stagnation, or at least a marked reduction, in bile secretion and flow. Cholestasis can be due to a functional impairment of ... Read the Article | 1 | 6 | Activity MD/PA |
| Chondroblastoma | Chondroblastoma is a benign, chondroid-producing neoplasm composed of chondroblasts. It accounts for less than 1% of all bone tumors and usually arise ... Read the Article | 1.25 | 10 | Activity DO |
| Chondroblastoma | Chondroblastoma is a benign, chondroid-producing neoplasm composed of chondroblasts. It accounts for less than 1% of all bone tumors and usually arise ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Chromhidrosis | Chromhidrosis is a rare condition with a characteristic presentation of the secretion of colored sweat. This condition can further subdivide into apoc ... Read the Article | 1 | 5 | Activity DO |
| Chromhidrosis | Chromhidrosis is a rare condition with a characteristic presentation of the secretion of colored sweat. This condition can further subdivide into apoc ... Read the Article | 1 | 5 | 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 |
| Ciliary Dysfunction | The majority of newborns with primary ciliary dyskinesia (PCD), formerly known as immotile cilia syndrome, develop neonatal respiratory distress with ... Read the Article | 1.25 | 8 | Activity DO |
| Ciliary Dysfunction | The majority of newborns with primary ciliary dyskinesia (PCD), formerly known as immotile cilia syndrome, develop neonatal respiratory distress with ... Read the Article | 1.25 | 8 | 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 |
| Clinodactyly | Clinodactyly is defined as a congenital curvature of a digit distal to the metacarpal phalangeal joint in the coronal plane. Curvatures with an angula ... Read the Article | 1 | 6 | Activity DO |
| Clinodactyly | Clinodactyly is defined as a congenital curvature of a digit distal to the metacarpal phalangeal joint in the coronal plane. Curvatures with an angula ... Read the Article | 1 | 6 | 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 |
| Complement Deficiency | The complement system is a crucial part of the innate humoral immune system. The purpose of the complement system is to orchestrate opsonization, faci ... Read the Article | 1.25 | 8 | Activity DO |
| Complement Deficiency | The complement system is a crucial part of the innate humoral immune system. The purpose of the complement system is to orchestrate opsonization, faci ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Conductive Hearing Loss | Conductive hearing loss encompasses a wide range of pathologies that affect patients of all ages. It can be the result of a defect anywhere from the e ... Read the Article | 1 | 3 | Activity DO |
| Conductive Hearing Loss | Conductive hearing loss encompasses a wide range of pathologies that affect patients of all ages. It can be the result of a defect anywhere from the e ... Read the Article | 1 | 3 | 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 | 1.25 | 10 | 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 | 1.25 | 10 | 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 | 10 | 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 | 10 | 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 | 4 | 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 | 4 | 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 Smooth Muscle Hamartoma | Congenital smooth muscle hamartoma is a benign proliferation of smooth muscle cells, organized in haphazardly-oriented bundles among the reticular der ... Read the Article | 1 | 6 | Activity DO |
| Congenital Smooth Muscle Hamartoma | Congenital smooth muscle hamartoma is a benign proliferation of smooth muscle cells, organized in haphazardly-oriented bundles among the reticular der ... Read the Article | 1 | 6 | 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 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 |
| Cooley Anemia | Thalassemia major or Cooley anemia is one of the common monogenic hereditary hemoglobin disorders. It results from the absence of a beta-globin chain ... Read the Article | 1 | 6 | Activity DO |
| Cooley Anemia | Thalassemia major or Cooley anemia is one of the common monogenic hereditary hemoglobin disorders. It results from the absence of a beta-globin chain ... Read the Article | 1 | 6 | 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 Arteriovenous Fistula | Coronary arteriovenous fistula should be suspected in patients who present with unexplained heart failure, have continuous murmur on auscultation, and ... Read the Article | 1 | 5 | Activity DO |
| Coronary Arteriovenous Fistula | Coronary arteriovenous fistula should be suspected in patients who present with unexplained heart failure, have continuous murmur on auscultation, and ... Read the Article | 1 | 5 | Activity MD/PA |
| Corynebacterium Diphtheriae | Pharyngitis is defined as the inflammation of pharyngeal tissue. Based on etiology, it can be divided into infectious and non-infectious sources. Vira ... Read the Article | 1.25 | 10 | Activity DO |
| Corynebacterium Diphtheriae | Pharyngitis is defined as the inflammation of pharyngeal tissue. Based on etiology, it can be divided into infectious and non-infectious sources. Vira ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Cow Milk Allergy | Cow's milk allergy is an allergic reaction to the protein found in cow’s milk. Diagnosis can be difficult as it is primarily based on history and phys ... Read the Article | 1 | 6 | Activity DO |
| Cow Milk Allergy | Cow's milk allergy is an allergic reaction to the protein found in cow’s milk. Diagnosis can be difficult as it is primarily based on history and phys ... Read the Article | 1 | 6 | 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 |
| Cutis Laxa | Cutis laxa (CL) is a group of rare diseases of connective tissue characterized by redundant skin with loss of elasticity and premature aging. Heritabl ... Read the Article | 1 | 5 | Activity DO |
| Cutis Laxa | Cutis laxa (CL) is a group of rare diseases of connective tissue characterized by redundant skin with loss of elasticity and premature aging. Heritabl ... Read the Article | 1 | 5 | 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 |
| 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 |
| Cyclic Neutropenia | Cyclic neutropenia is a very rare hematological condition characterized by regular fluctuations in blood neutrophil counts, leading to periodic neutro ... Read the Article | 1 | 5 | Activity DO |
| Cyclic Neutropenia | Cyclic neutropenia is a very rare hematological condition characterized by regular fluctuations in blood neutrophil counts, leading to periodic neutro ... Read the Article | 1 | 5 | 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 | 43 | 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 | 43 | Activity MD/PA |
| Cystic Fibrosis Related Diabetes | Cystic fibrosis-related diabetes is an extrapulmonary complication of cystic fibrosis. Cystic fibrosis-related diabetes is the result of abnormal gluc ... Read the Article | 1 | 5 | Activity DO |
| Cystic Fibrosis Related Diabetes | Cystic fibrosis-related diabetes is an extrapulmonary complication of cystic fibrosis. Cystic fibrosis-related diabetes is the result of abnormal gluc ... Read the Article | 1 | 5 | 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 |
| Cystinuria | Cystine stones are due to an inherited defect in the transport of the amino acid cystine leading to excessive excretion in the kidney causing cystinur ... Read the Article | 1 | 5 | Activity DO |
| Cystinuria | Cystine stones are due to an inherited defect in the transport of the amino acid cystine leading to excessive excretion in the kidney causing cystinur ... Read the Article | 1 | 5 | Activity MD/PA |
| Deep Neck Infections | Deep neck infections are a serious but treatable group of infections affecting the deep cervical space and characterized by rapid progression and life ... Read the Article | 1 | 5 | Activity DO |
| Deep Neck Infections | Deep neck infections are a serious but treatable group of infections affecting the deep cervical space and characterized by rapid progression and life ... Read the Article | 1 | 5 | Activity MD/PA |
| Dermatitis Herpetiformis | Dermatitis herpetiformis is a chronic, autoimmune, blistering disease that causes an extremely pruritic rash that predominantly affects the extensor s ... Read the Article | 1.25 | 13 | Activity DO |
| Dermatitis Herpetiformis | Dermatitis herpetiformis is a chronic, autoimmune, blistering disease that causes an extremely pruritic rash that predominantly affects the extensor s ... Read the Article | 1.25 | 13 | Activity MD/PA |
| Dermatographism | Dermatographism, also known as dermographism urticaria, or urticaria factitia, is an urticarial eruption upon pressure or trauma to the skin. The lite ... Read the Article | 1 | 4 | Activity DO |
| Dermatographism | Dermatographism, also known as dermographism urticaria, or urticaria factitia, is an urticarial eruption upon pressure or trauma to the skin. The lite ... Read the Article | 1 | 4 | Activity MD/PA |
| Diffuse Intrinsic Pontine Glioma | Diffuse intrinsic pontine glioma (DIPG) is an aggressive type of childhood cancer that forms in the brainstem. They are very rare and almost always oc ... Read the Article | 1 | 5 | Activity DO |
| Diffuse Intrinsic Pontine Glioma | Diffuse intrinsic pontine glioma (DIPG) is an aggressive type of childhood cancer that forms in the brainstem. They are very rare and almost always oc ... 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 |
| Double Aortic Arch | Double aortic arch is the commonest form of a group of defects that affect the development of the aorta. This defect causes an abnormal circular forma ... Read the Article | 1 | 5 | Activity DO |
| Double Aortic Arch | Double aortic arch is the commonest form of a group of defects that affect the development of the aorta. This defect causes an abnormal circular forma ... Read the Article | 1 | 5 | Activity MD/PA |
| Double Orifice Mitral Valve | A double orifice mitral valve (DOMV) is a rare, congenital, or acquired anomaly that is typically asymptomatic. With time, however, it may lead to mit ... Read the Article | 1 | 4 | Activity DO |
| Double Orifice Mitral Valve | A double orifice mitral valve (DOMV) is a rare, congenital, or acquired anomaly that is typically asymptomatic. With time, however, it may lead to mit ... Read the Article | 1 | 4 | 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 | 14 | 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 | 14 | Activity MD/PA |
| Duchenne Muscular Dystrophy | Unfortunately, Duchenne muscular dystrophy (DMD) is not only one of the most severe forms of inherited muscular dystrophies but also the most common h ... Read the Article | 1.75 | 24 | Activity DO |
| Duchenne Muscular Dystrophy | Unfortunately, Duchenne muscular dystrophy (DMD) is not only one of the most severe forms of inherited muscular dystrophies but also the most common h ... Read the Article | 1.75 | 24 | Activity MD/PA |
| Ear Microtia | Microtia is a congenital ear deformity in which the external ear is malformed and underdeveloped. In more severe cases, it is usually associated with ... Read the Article | 1.25 | 7 | Activity DO |
| Ear Microtia | Microtia is a congenital ear deformity in which the external ear is malformed and underdeveloped. In more severe cases, it is usually associated with ... Read the Article | 1.25 | 7 | 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 |
| Eczema Herpeticum | Eczema herpeticum (EH) is a disseminated cutaneous infection with herpes simplex virus that develops in a patient with atopic dermatitis. EH typically ... Read the Article | 1 | 7 | Activity DO |
| Eczema Herpeticum | Eczema herpeticum (EH) is a disseminated cutaneous infection with herpes simplex virus that develops in a patient with atopic dermatitis. EH typically ... Read the Article | 1 | 7 | 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 |
| 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 |
| Enchondroma | Enchondromas are benign tumors of unknown etiology that occur in the hyaline cartilage in bones of endochondral origin. Enchondromas account for appro ... Read the Article | 1 | 7 | Activity DO |
| Enchondroma | Enchondromas are benign tumors of unknown etiology that occur in the hyaline cartilage in bones of endochondral origin. Enchondromas account for appro ... Read the Article | 1 | 7 | Activity MD/PA |
| Endocardial Fibroelastosis | Endocardial fibroelastosis (EFE) is primarily a disease of infants and children, but can rarely present in adulthood as well. In 1943, the endocardial ... Read the Article | 1 | 5 | Activity DO |
| Endocardial Fibroelastosis | Endocardial fibroelastosis (EFE) is primarily a disease of infants and children, but can rarely present in adulthood as well. In 1943, the endocardial ... Read the Article | 1 | 5 | Activity MD/PA |
| Endovascular Papillary Angioendothelioma | Endovascular papillary angioendothelioma (EPA), also known as Dabska tumor (DT) and papillary intralymphatic angioendothelioma (PILA), represents a bo ... Read the Article | 1.25 | 10 | Activity DO |
| Endovascular Papillary Angioendothelioma | Endovascular papillary angioendothelioma (EPA), also known as Dabska tumor (DT) and papillary intralymphatic angioendothelioma (PILA), represents a bo ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Enterovirus | Enteroviruses are a class of viruses comprising over 300 serotypes. These ubiquitous viruses cause a wide spectrum of diseases with heterogeneous pres ... Read the Article | 1 | 5 | Activity DO |
| Enterovirus | Enteroviruses are a class of viruses comprising over 300 serotypes. These ubiquitous viruses cause a wide spectrum of diseases with heterogeneous pres ... Read the Article | 1 | 5 | Activity MD/PA |
| Entomophthoromycosis | Entomophthoromycosis is a fungal infection involving the skin and subcutaneous tissues. It is generally not life-threatening but can lead to prolonged ... Read the Article | 1 | 5 | Activity DO |
| Entomophthoromycosis | Entomophthoromycosis is a fungal infection involving the skin and subcutaneous tissues. It is generally not life-threatening but can lead to prolonged ... Read the Article | 1 | 5 | Activity MD/PA |
| Eosinophilic Gastroenteritis | Eosinophilic gastroenteritis belongs to the group of eosinophilic gastrointestinal disorders, which comprise eosinophilic esophagitis and eosinophilic ... Read the Article | 1 | 4 | Activity DO |
| Eosinophilic Gastroenteritis | Eosinophilic gastroenteritis belongs to the group of eosinophilic gastrointestinal disorders, which comprise eosinophilic esophagitis and eosinophilic ... Read the Article | 1 | 4 | Activity MD/PA |
| Eosinophilic Granuloma | Eosinophilic granuloma (EG) is a rare and mildest form of Langerhans cell histiocytosis. The presentation of EG can be monostotic, polyostotic, or can ... Read the Article | 1.25 | 8 | Activity DO |
| Eosinophilic Granuloma | Eosinophilic granuloma (EG) is a rare and mildest form of Langerhans cell histiocytosis. The presentation of EG can be monostotic, polyostotic, or can ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Ependymoma | Ependymomas are glial cell tumors that commonly arise in the lining cells of the ventricular system, and less commonly outside the central nervous sys ... Read the Article | 1 | 7 | Activity DO |
| Ependymoma | Ependymomas are glial cell tumors that commonly arise in the lining cells of the ventricular system, and less commonly outside the central nervous sys ... Read the Article | 1 | 7 | 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 |
| 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 | 9 | 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 | 9 | 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 |
| Erythropoietic Protoporphyria | Erythropoietic protoporphyria (EPP) is an inherited porphyria resulting in the accumulation of protoporphyrins in red blood cells that causes acute, p ... Read the Article | 1 | 5 | Activity DO |
| Erythropoietic Protoporphyria | Erythropoietic protoporphyria (EPP) is an inherited porphyria resulting in the accumulation of protoporphyrins in red blood cells that causes acute, p ... Read the Article | 1 | 5 | Activity MD/PA |
| Ethylenediaminetetraacetic Acid (EDTA) | Ethylenediaminetetraacetic acid (EDTA) is a medication used in the management and treatment of heavy metal toxicity. It is in the chelating class of d ... Read the Article | 1 | 4 | Activity DO |
| Ethylenediaminetetraacetic Acid (EDTA) | Ethylenediaminetetraacetic acid (EDTA) is a medication used in the management and treatment of heavy metal toxicity. It is in the chelating class of d ... Read the Article | 1 | 4 | Activity MD/PA |
| Ewing Sarcoma | Ewing sarcoma is the second most common primary malignant bone tumor, mostly affecting adolescents in the second decade of their life, and it is a hig ... Read the Article | 1.5 | 15 | Activity DO |
| Ewing Sarcoma | Ewing sarcoma is the second most common primary malignant bone tumor, mostly affecting adolescents in the second decade of their life, and it is a hig ... Read the Article | 1.5 | 15 | 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 |
| 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 |
| Familial Short Stature | Familial short stature (FSS) is the condition characterized by the final adult height below the third percentile of the mean for the patient's age, ge ... Read the Article | 1 | 5 | Activity DO |
| Familial Short Stature | Familial short stature (FSS) is the condition characterized by the final adult height below the third percentile of the mean for the patient's age, ge ... Read the Article | 1 | 5 | Activity MD/PA |
| Fanconi Anemia | Fanconi anemia is a rare genetic disorder, involving all three blood cell lines. It is the most common cause of inherited bone marrow failure characte ... Read the Article | 1.25 | 8 | Activity DO |
| Fanconi Anemia | Fanconi anemia is a rare genetic disorder, involving all three blood cell lines. It is the most common cause of inherited bone marrow failure characte ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Fructose 1-Phosphate Aldolase Deficiency | Fructose 1-phosphate aldolase deficiency or hereditary fructose intolerance (HFI) is an autosomal recessive disorder caused by the deficiency in aldol ... Read the Article | 1 | 7 | Activity DO |
| Fructose 1-Phosphate Aldolase Deficiency | Fructose 1-phosphate aldolase deficiency or hereditary fructose intolerance (HFI) is an autosomal recessive disorder caused by the deficiency in aldol ... Read the Article | 1 | 7 | Activity MD/PA |
| Fungal Endocarditis | Endocarditis is the inflammation of the endocardium, the innermost lining of the heart. Endocarditis may be due to infective or non-infective etiologi ... Read the Article | 1 | 6 | Activity DO |
| Fungal Endocarditis | Endocarditis is the inflammation of the endocardium, the innermost lining of the heart. Endocarditis may be due to infective or non-infective etiologi ... Read the Article | 1 | 6 | Activity MD/PA |
| Germ Cell Seminoma | Germinoma is an uncommon pediatric brain tumor that is morphologically identical to its gonadal counterpart: testicular seminoma and ovarian dysgermin ... Read the Article | 1 | 7 | Activity DO |
| Germ Cell Seminoma | Germinoma is an uncommon pediatric brain tumor that is morphologically identical to its gonadal counterpart: testicular seminoma and ovarian dysgermin ... Read the Article | 1 | 7 | Activity MD/PA |
| Gitelman Syndrome | Gitelman syndrome is a salt-losing tubulopathy caused by mutation of genes encoding sodium chloride (NCCT) and magnesium transporters in the thiazide- ... Read the Article | 1 | 6 | Activity DO |
| Gitelman Syndrome | Gitelman syndrome is a salt-losing tubulopathy caused by mutation of genes encoding sodium chloride (NCCT) and magnesium transporters in the thiazide- ... Read the Article | 1 | 6 | Activity MD/PA |
| Glomus Cancer | Glomangioma or glomuvenous malformation is a rare cutaneous venous malformation that shows glomus cells (undifferentiated smooth muscle cells which ar ... Read the Article | 1 | 6 | Activity DO |
| Glomus Cancer | Glomangioma or glomuvenous malformation is a rare cutaneous venous malformation that shows glomus cells (undifferentiated smooth muscle cells which ar ... Read the Article | 1 | 6 | Activity MD/PA |
| Glucose 6 Phosphate Dehydrogenase Deficiency | Glucose-6-phosphate dehydrogenase is an enzyme found in the cytoplasm of all cells in the body. It is a housekeeping enzyme that plays a vital role in ... Read the Article | 1 | 5 | Activity DO |
| Glucose 6 Phosphate Dehydrogenase Deficiency | Glucose-6-phosphate dehydrogenase is an enzyme found in the cytoplasm of all cells in the body. It is a housekeeping enzyme that plays a vital role in ... Read the Article | 1 | 5 | Activity MD/PA |
| Glycogen Storage Disease | Glycogen storage diseases (GSDs) are inherited inborn errors of metabolism of carbohydrates. In general, these results from a lack of specific enzymes ... Read the Article | 1.25 | 8 | Activity DO |
| Glycogen Storage Disease | Glycogen storage diseases (GSDs) are inherited inborn errors of metabolism of carbohydrates. In general, these results from a lack of specific enzymes ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Glycogenic Hepatopathy | Glycogenic hepatopathy (GH) is a rare or possibly under-diagnosed complication seen in children and young adults with poorly controlled type 1 diabete ... Read the Article | 1 | 6 | Activity DO |
| Glycogenic Hepatopathy | Glycogenic hepatopathy (GH) is a rare or possibly under-diagnosed complication seen in children and young adults with poorly controlled type 1 diabete ... Read the Article | 1 | 6 | Activity MD/PA |
| Gorlin Syndrome | Gorlin syndrome, also called Gorlin-Goltz syndrome, basal cell nevus syndrome (BCNS), or nevoid basal cell carcinoma syndrome, is an autosomal dominan ... Read the Article | 1 | 5 | Activity DO |
| Gorlin Syndrome | Gorlin syndrome, also called Gorlin-Goltz syndrome, basal cell nevus syndrome (BCNS), or nevoid basal cell carcinoma syndrome, is an autosomal dominan ... Read the Article | 1 | 5 | Activity MD/PA |
| Graft Versus Host Disease | Graft-versus-host disease (GVHD) occurs due to the presence of immunocompetent T lymphocytes in the graft attacking the immunodeficient recipient tiss ... Read the Article | 1 | 7 | Activity DO |
| Graft Versus Host Disease | Graft-versus-host disease (GVHD) occurs due to the presence of immunocompetent T lymphocytes in the graft attacking the immunodeficient recipient tiss ... Read the Article | 1 | 7 | Activity MD/PA |
| Gram Positive Bacteria | Gram-positive organisms have highly variable growth and resistance patterns. The SCOPE project (Surveillance and Control of Pathogens of Epidemiologic ... Read the Article | 1 | 5 | Activity DO |
| Gram Positive Bacteria | Gram-positive organisms have highly variable growth and resistance patterns. The SCOPE project (Surveillance and Control of Pathogens of Epidemiologic ... Read the Article | 1 | 5 | Activity MD/PA |
| Granuloma Annulare | Granuloma annulare is a cutaneous granulomatous disease that is not caused by an infection. It is the most common non-infectious granulomatous disease ... Read the Article | 1 | 6 | Activity DO |
| Granuloma Annulare | Granuloma annulare is a cutaneous granulomatous disease that is not caused by an infection. It is the most common non-infectious granulomatous disease ... Read the Article | 1 | 6 | Activity MD/PA |
| Guillain Barre Syndrome | Guillain-Barre syndrome (GBS) is a rare but serious post-infectious immune-mediated neuropathy. It results from the autoimmune destruction of nerves i ... Read the Article | 1.75 | 21 | Activity DO |
| Guillain Barre Syndrome | Guillain-Barre syndrome (GBS) is a rare but serious post-infectious immune-mediated neuropathy. It results from the autoimmune destruction of nerves i ... Read the Article | 1.75 | 21 | Activity MD/PA |
| Gyrate Atrophy Of The Choroid and Retina | Gyrate atrophy of the choroid and retina is a rare autosomal recessive condition characterized by elevation of plasma ornithine levels due to deficien ... Read the Article | 1 | 5 | Activity DO |
| Gyrate Atrophy Of The Choroid and Retina | Gyrate atrophy of the choroid and retina is a rare autosomal recessive condition characterized by elevation of plasma ornithine levels due to deficien ... Read the Article | 1 | 5 | Activity MD/PA |
| H1N1 Influenza | H1N1 influenza is a subtype of influenza A virus, a communicable viral illness which causes upper and in some cases lower respiratory tract infections ... Read the Article | 1 | 4 | Activity DO |
| H1N1 Influenza | H1N1 influenza is a subtype of influenza A virus, a communicable viral illness which causes upper and in some cases lower respiratory tract infections ... Read the Article | 1 | 4 | Activity MD/PA |
| Hallervorden Spatz Disease | Hallervorden-Spatz disease now known as pantothenate kinase-associated neurodegeneration (PKAN) is a rare autosomal recessive neurodegenerative disord ... Read the Article | 1 | 5 | Activity DO |
| Hallervorden Spatz Disease | Hallervorden-Spatz disease now known as pantothenate kinase-associated neurodegeneration (PKAN) is a rare autosomal recessive neurodegenerative disord ... Read the Article | 1 | 5 | Activity MD/PA |
| Heavy Metal Toxicity | Heavy metals are elements found in nature that accumulate in the environment mostly due to anthropogenic activities. Humans are exposed to them by occ ... Read the Article | 1 | 5 | Activity DO |
| Heavy Metal Toxicity | Heavy metals are elements found in nature that accumulate in the environment mostly due to anthropogenic activities. Humans are exposed to them by occ ... Read the Article | 1 | 5 | Activity MD/PA |
| Hemangioma | Hemangiomas, colloquially termed "strawberry marks", are the most common benign tumor of infancy and are caused by endothelial cell proliferation. Con ... Read the Article | 1.25 | 12 | Activity DO |
| Hemangioma | Hemangiomas, colloquially termed "strawberry marks", are the most common benign tumor of infancy and are caused by endothelial cell proliferation. Con ... Read the Article | 1.25 | 12 | Activity MD/PA |
| Hemolytic Uremic Syndrome | Hemolytic uremic syndrome (HUS) is thrombotic microangiopathy characterized by the presence of a triad of symptoms: thrombocytopenia, acute renal impa ... Read the Article | 1.25 | 9 | Activity DO |
| Hemolytic Uremic Syndrome | Hemolytic uremic syndrome (HUS) is thrombotic microangiopathy characterized by the presence of a triad of symptoms: thrombocytopenia, acute renal impa ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Hemophilia A | Hemophilia encompasses a group of inherited disorders that alter blood coagulation. Classical hemophilia, also known as hemophilia A, is a hereditary ... Read the Article | 1.25 | 12 | Activity DO |
| Hemophilia A | Hemophilia encompasses a group of inherited disorders that alter blood coagulation. Classical hemophilia, also known as hemophilia A, is a hereditary ... Read the Article | 1.25 | 12 | 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 |
| Hereditary Fructose Intolerance | Hereditary fructose intolerance is an autosomal recessive disorder where patients lack the enzyme to break down fructose-1-phosphate. This disease usu ... Read the Article | 1 | 5 | Activity DO |
| Hereditary Fructose Intolerance | Hereditary fructose intolerance is an autosomal recessive disorder where patients lack the enzyme to break down fructose-1-phosphate. This disease usu ... Read the Article | 1 | 5 | Activity MD/PA |
| Hereditary Sitosterolemia | Sitosterolemia is an inherited condition that can lead to premature heart disease and other complications. It is characterized by excess accumulation ... Read the Article | 1.25 | 10 | Activity DO |
| Hereditary Sitosterolemia | Sitosterolemia is an inherited condition that can lead to premature heart disease and other complications. It is characterized by excess accumulation ... Read the Article | 1.25 | 10 | 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 |
| Hodgkin Lymphoma | Hodgkin lymphoma (HL) is a rare monoclonal lymphoid neoplasm characterized by the following four features: HL usually presents in young adults, common ... Read the Article | 1.25 | 10 | Activity DO |
| Hodgkin Lymphoma | Hodgkin lymphoma (HL) is a rare monoclonal lymphoid neoplasm characterized by the following four features: HL usually presents in young adults, common ... Read the Article | 1.25 | 10 | 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 |
| Hydronephrosis And Hydroureter | Hydronephrosis and hydroureter result from obstruction of urine flow in the urinary system at the renal pelvis and ureter level, respectively. This is ... Read the Article | 1 | 6 | Activity DO |
| Hydronephrosis And Hydroureter | Hydronephrosis and hydroureter result from obstruction of urine flow in the urinary system at the renal pelvis and ureter level, respectively. This is ... Read the Article | 1 | 6 | Activity MD/PA |
| Hyperkalemic Periodic Paralysis | Hyperkalemic periodic paralysis is a rare condition presenting as temporary periods of severe muscle weakness or paralysis. To treat this condition ap ... Read the Article | 1 | 6 | Activity DO |
| Hyperkalemic Periodic Paralysis | Hyperkalemic periodic paralysis is a rare condition presenting as temporary periods of severe muscle weakness or paralysis. To treat this condition ap ... Read the Article | 1 | 6 | Activity MD/PA |
| Hyperphosphatemia | This article summarises the basics of Hyperphosphatemia, including its pathophysiology, evaluation, and management. Though this condition is seen more ... Read the Article | 1 | 6 | Activity DO |
| Hyperphosphatemia | This article summarises the basics of Hyperphosphatemia, including its pathophysiology, evaluation, and management. Though this condition is seen more ... Read the Article | 1 | 6 | Activity MD/PA |
| Hyperphosphatemic Tumoral Calcinosis | Hyperphosphatemic tumoral calcinosis is a disorder of phosphate regulation caused due to a defect in the functioning of fibroblast growth factor-23 an ... Read the Article | 1 | 5 | Activity DO |
| Hyperphosphatemic Tumoral Calcinosis | Hyperphosphatemic tumoral calcinosis is a disorder of phosphate regulation caused due to a defect in the functioning of fibroblast growth factor-23 an ... Read the Article | 1 | 5 | Activity MD/PA |
| Hypogammaglobulinemia | Hypogammaglobulinemia is a disorder caused by low serum immunoglobulin or antibody levels. Immunoglobulins are the main components of the humoral immu ... Read the Article | 1.25 | 9 | Activity DO |
| Hypogammaglobulinemia | Hypogammaglobulinemia is a disorder caused by low serum immunoglobulin or antibody levels. Immunoglobulins are the main components of the humoral immu ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Hypokalemic Metabolic Alkalosis | Since the first step out of the marine world, the animals had to adapt to the lack of fluid and electrolytes found in abundance in seawater. Over time ... Read the Article | 1 | 4 | Activity DO |
| Hypokalemic Metabolic Alkalosis | Since the first step out of the marine world, the animals had to adapt to the lack of fluid and electrolytes found in abundance in seawater. Over time ... Read the Article | 1 | 4 | Activity MD/PA |
| Hypokalemic Periodic Paralysis | Hypokalemic periodic paralysis is a rare channelopathy caused by the skeletal muscle ion channel mutations, commonly calcium channel and less commonly ... Read the Article | 1.25 | 7 | Activity DO |
| Hypokalemic Periodic Paralysis | Hypokalemic periodic paralysis is a rare channelopathy caused by the skeletal muscle ion channel mutations, commonly calcium channel and less commonly ... Read the Article | 1.25 | 7 | Activity MD/PA |
| Hypophosphatemia | Given its widespread role in nearly every molecular, cellular function, aberrations in serum phosphate levels can be highly impactful. Hypophosphatemi ... Read the Article | 1 | 5 | Activity DO |
| Hypophosphatemia | Given its widespread role in nearly every molecular, cellular function, aberrations in serum phosphate levels can be highly impactful. Hypophosphatemi ... Read the Article | 1 | 5 | Activity MD/PA |
| Hypopigmented Macules | Hypopigmented macules are one of the most common skin lesions encountered in clinical practice. As the name suggests, these lesions are associated wit ... Read the Article | 1 | 6 | Activity DO |
| Hypopigmented Macules | Hypopigmented macules are one of the most common skin lesions encountered in clinical practice. As the name suggests, these lesions are associated wit ... Read the Article | 1 | 6 | Activity MD/PA |
| Hypothalamic Dysfunction | The hypothalamus is the central command center for hormonal regulation, and its effects are primarily carried out by the hormones released from the hy ... Read the Article | 1 | 5 | Activity DO |
| Hypothalamic Dysfunction | The hypothalamus is the central command center for hormonal regulation, and its effects are primarily carried out by the hormones released from the hy ... Read the Article | 1 | 5 | 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 |
| 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 |
| Immunoglobulin | Immunoglobulins (Ig) or antibodies are glycoproteins that are produced by plasma cells. B cells are instructed by specific immunogens, for, example, b ... Read the Article | 1.25 | 9 | Activity DO |
| Immunoglobulin | Immunoglobulins (Ig) or antibodies are glycoproteins that are produced by plasma cells. B cells are instructed by specific immunogens, for, example, b ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Immunotherapy | Immunotherapy is used to upregulate or downregulate the immune system to achieve a therapeutic effect in immunological mediated disorders, including i ... Read the Article | 1.25 | 8 | Activity DO |
| Immunotherapy | Immunotherapy is used to upregulate or downregulate the immune system to achieve a therapeutic effect in immunological mediated disorders, including i ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Inborn Errors Of Metabolism | Inborn errors of metabolism are a heterogeneous group of disorders that may be inherited or may occur as the result of spontaneous mutations. These di ... Read the Article | 1 | 8 | Activity DO |
| Inborn Errors Of Metabolism | Inborn errors of metabolism are a heterogeneous group of disorders that may be inherited or may occur as the result of spontaneous mutations. These di ... 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 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 |
| Intestinal And Multivisceral Transplantation | Organ transplantation has quickly developed into a dynamic field in medicine that involves a large multidisciplinary team to manage patients care in t ... Read the Article | 1 | 5 | Activity DO |
| Intestinal And Multivisceral Transplantation | Organ transplantation has quickly developed into a dynamic field in medicine that involves a large multidisciplinary team to manage patients care in t ... Read the Article | 1 | 5 | Activity MD/PA |
| Inverted Urothelial Papilloma | Inverted urothelial papilloma is a rare non-invasive endophytic urothelial tumor of the urinary bladder accounting for less than 1% of urothelial neop ... Read the Article | 1 | 5 | Activity DO |
| Inverted Urothelial Papilloma | Inverted urothelial papilloma is a rare non-invasive endophytic urothelial tumor of the urinary bladder accounting for less than 1% of urothelial neop ... Read the Article | 1 | 5 | Activity MD/PA |
| Jacobs Syndrome | Jacob's syndrome is a rare genetic abnormality in which a male receives an extra Y chromosome from his father. While many patients go undiagnosed due ... Read the Article | 1 | 7 | Activity DO |
| Jacobs Syndrome | Jacob's syndrome is a rare genetic abnormality in which a male receives an extra Y chromosome from his father. While many patients go undiagnosed due ... Read the Article | 1 | 7 | Activity MD/PA |
| Juvenile Xanthogranuloma | Juvenile xanthogranuloma (JXG) is a non-Langerhans cell histiocytosis and is fairly common, often affecting infants and young children. Cutaneous lesi ... Read the Article | 1 | 6 | Activity DO |
| Juvenile Xanthogranuloma | Juvenile xanthogranuloma (JXG) is a non-Langerhans cell histiocytosis and is fairly common, often affecting infants and young children. Cutaneous lesi ... Read the Article | 1 | 6 | Activity MD/PA |
| Kawasaki Disease | Kawasaki disease (KD) is an acute, self-limited medium vessel vasculitis that has a predilection for the coronary arteries. This activity reviews the ... Read the Article | 1.75 | 19 | Activity DO |
| Kawasaki Disease | Kawasaki disease (KD) is an acute, self-limited medium vessel vasculitis that has a predilection for the coronary arteries. This activity reviews the ... Read the Article | 1.75 | 19 | Activity MD/PA |
| Kayser-Fleischer Ring | Kayser–Fleischer (KF) rings are a common ophthalmologic finding in patients with Wilson disease. Initially thought to be due to the accumulation of si ... Read the Article | 1 | 5 | Activity DO |
| Kayser-Fleischer Ring | Kayser–Fleischer (KF) rings are a common ophthalmologic finding in patients with Wilson disease. Initially thought to be due to the accumulation of si ... Read the Article | 1 | 5 | Activity MD/PA |
| Ketoacidosis | Ketoacidosis is a metabolic state associated with pathologically high serum and urine concentrations of ketone bodies. Clinically relevant forms of ke ... Read the Article | 1.25 | 7 | Activity DO |
| Ketoacidosis | Ketoacidosis is a metabolic state associated with pathologically high serum and urine concentrations of ketone bodies. Clinically relevant forms of ke ... Read the Article | 1.25 | 7 | Activity MD/PA |
| Kingella Kingae | This activity reviews the microbiology, epidemiology, pathophysiology and the clinical manifestations of Kingella kingae infection. It also highlights ... Read the Article | 1 | 5 | Activity DO |
| Kingella Kingae | This activity reviews the microbiology, epidemiology, pathophysiology and the clinical manifestations of Kingella kingae infection. It also highlights ... 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 |
| Krabbe Disease | Krabbe disease, an autosomal recessive disease, is a type of lysosomal storage disorder that results from the deficiency of the enzyme galactocerebros ... Read the Article | 1 | 6 | Activity DO |
| Krabbe Disease | Krabbe disease, an autosomal recessive disease, is a type of lysosomal storage disorder that results from the deficiency of the enzyme galactocerebros ... Read the Article | 1 | 6 | Activity MD/PA |
| La Crosse Encephalitis | La Crosse encephalitis is a relatively uncommon arboviral illness predominantly seen in the pediatric population but may also affect adults. Though no ... Read the Article | 1 | 4 | Activity DO |
| La Crosse Encephalitis | La Crosse encephalitis is a relatively uncommon arboviral illness predominantly seen in the pediatric population but may also affect adults. Though no ... Read the Article | 1 | 4 | Activity MD/PA |
| Leishmaniasis | Leishmaniasis is a protozoan disease transmitted by sandflies that is most commonly seen in Europe, Africa, Asia, and Latin America. As travel pattern ... Read the Article | 1.25 | 9 | Activity DO |
| Leishmaniasis | Leishmaniasis is a protozoan disease transmitted by sandflies that is most commonly seen in Europe, Africa, Asia, and Latin America. As travel pattern ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Leptospirosis | Leptospirosis, also called Weil disease, is the most common zoonotic infection in the world. Leptospirosis is caused by an infection with the spiroche ... Read the Article | 1.25 | 11 | Activity DO |
| Leptospirosis | Leptospirosis, also called Weil disease, is the most common zoonotic infection in the world. Leptospirosis is caused by an infection with the spiroche ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Leukocytoclastic Vasculitis | Leukocytoclastic vasculitis is a cutaneous, small-vessel vasculitis of the dermal capillaries and venules. This condition can be idiopathic or can be ... Read the Article | 1 | 6 | Activity DO |
| Leukocytoclastic Vasculitis | Leukocytoclastic vasculitis is a cutaneous, small-vessel vasculitis of the dermal capillaries and venules. This condition can be idiopathic or can be ... Read the Article | 1 | 6 | Activity MD/PA |
| Lipoid Proteinosis | Lipoid proteinosis is an autosomal recessive condition characterized by hyaline-like deposits in the skin, mucous membranes, and other parts of the bo ... Read the Article | 1 | 5 | Activity DO |
| Lipoid Proteinosis | Lipoid proteinosis is an autosomal recessive condition characterized by hyaline-like deposits in the skin, mucous membranes, and other parts of the bo ... Read the Article | 1 | 5 | Activity MD/PA |
| Lisch Nodules | Lisch nodules, traditionally described as iris hamartomas is one of the pathognomic markers of neurofibromatosis type 1 (NF1) and are rarely seen in i ... Read the Article | 1 | 7 | Activity DO |
| Lisch Nodules | Lisch nodules, traditionally described as iris hamartomas is one of the pathognomic markers of neurofibromatosis type 1 (NF1) and are rarely seen in i ... Read the Article | 1 | 7 | Activity MD/PA |
| Loose Anagen Syndrome | Loose anagen syndrome is inherited in an autosomal dominant or sporadic fashion. Clinically it manifests as diffuse non-scarring alopecia in children. ... Read the Article | 1 | 6 | Activity DO |
| Loose Anagen Syndrome | Loose anagen syndrome is inherited in an autosomal dominant or sporadic fashion. Clinically it manifests as diffuse non-scarring alopecia in children. ... Read the Article | 1 | 6 | Activity MD/PA |
| Lymphohistiocytosis | Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening, hyper-inflammatory disorder affecting both newborns and adults alike. The disease is c ... Read the Article | 1 | 5 | Activity DO |
| Lymphohistiocytosis | Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening, hyper-inflammatory disorder affecting both newborns and adults alike. The disease is c ... Read the Article | 1 | 5 | Activity MD/PA |
| Macroglossia | Macroglossia is usually seen in association with genetic syndromes. Macroglossia can be congenital or acquired. Congenital macroglossia is an uncommon ... Read the Article | 1 | 6 | Activity DO |
| Macroglossia | Macroglossia is usually seen in association with genetic syndromes. Macroglossia can be congenital or acquired. Congenital macroglossia is an uncommon ... Read the Article | 1 | 6 | Activity MD/PA |
| Mantle Cell Lymphoma | Mantle cell lymphoma (MCL) is a rare subtype of B-cell non-Hodgkin lymphomas (NHLs) defined by a confirmatory translocation of the CCND1 gene. The va ... Read the Article | 1 | 5 | Activity DO |
| Mantle Cell Lymphoma | Mantle cell lymphoma (MCL) is a rare subtype of B-cell non-Hodgkin lymphomas (NHLs) defined by a confirmatory translocation of the CCND1 gene. The va ... Read the Article | 1 | 5 | Activity MD/PA |
| Marfan Syndrome | One of the most common inherited disorders affecting connective tissue, Marfan syndrome (MFS) is an autosomal dominant condition with a reported incid ... Read the Article | 1.5 | 12 | Activity DO |
| Marfan Syndrome | One of the most common inherited disorders affecting connective tissue, Marfan syndrome (MFS) is an autosomal dominant condition with a reported incid ... Read the Article | 1.5 | 12 | Activity MD/PA |
| Mastocytoma | A mastocytoma is a tumor of mast cells, which are derived from myeloid stem cells and located in connective tissues, predominantly in the skin and muc ... Read the Article | 1 | 6 | Activity DO |
| Mastocytoma | A mastocytoma is a tumor of mast cells, which are derived from myeloid stem cells and located in connective tissues, predominantly in the skin and muc ... Read the Article | 1 | 6 | Activity MD/PA |
| Maturity Onset Diabetes in the Young | The most commonly recognized forms of diabetes mellitus include type 1 diabetes, an autoimmune disorder, and type 2 diabetes, a polygenic disorder inf ... Read the Article | 1.25 | 8 | Activity DO |
| Maturity Onset Diabetes in the Young | The most commonly recognized forms of diabetes mellitus include type 1 diabetes, an autoimmune disorder, and type 2 diabetes, a polygenic disorder inf ... Read the Article | 1.25 | 8 | Activity MD/PA |
| McArdle Disease | McArdle disease is a genetic disorder that mainly affects skeletal muscles. It occurs due to the deficiency or absence of an enzyme called myophosphor ... Read the Article | 1 | 6 | Activity DO |
| McArdle Disease | McArdle disease is a genetic disorder that mainly affects skeletal muscles. It occurs due to the deficiency or absence of an enzyme called myophosphor ... Read the Article | 1 | 6 | Activity MD/PA |
| McCune Albright Syndrome | McCune-Albright syndrome is a rare genetic disordered originally recognized by the triad of polyostotic fibrous dysplasia, precocious puberty, and caf ... Read the Article | 1 | 6 | Activity DO |
| McCune Albright Syndrome | McCune-Albright syndrome is a rare genetic disordered originally recognized by the triad of polyostotic fibrous dysplasia, precocious puberty, and caf ... Read the Article | 1 | 6 | Activity MD/PA |
| Mean Corpuscular Volume | Mean corpuscular volume (MCV) is a measure used to determine anemia etiologies. This activity illustrates the categories of anemia with varying MCVs, ... Read the Article | 1 | 5 | Activity DO |
| Mean Corpuscular Volume | Mean corpuscular volume (MCV) is a measure used to determine anemia etiologies. This activity illustrates the categories of anemia with varying MCVs, ... Read the Article | 1 | 5 | Activity MD/PA |
| Meckel Diverticulum | Meckel diverticulum is a common congenital abnormality of the small intestine caused by incomplete obliteration of the vitelline (omphalomesenteric) d ... Read the Article | 1.5 | 17 | Activity DO |
| Meckel Diverticulum | Meckel diverticulum is a common congenital abnormality of the small intestine caused by incomplete obliteration of the vitelline (omphalomesenteric) d ... Read the Article | 1.5 | 17 | 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 |
| Medullary Sponge Kidney | Medullary sponge kidney is a benign congenital abnormality that was first described in 1939. Anatomically it is characterized by cystic dilatation of ... Read the Article | 1.25 | 9 | Activity DO |
| Medullary Sponge Kidney | Medullary sponge kidney is a benign congenital abnormality that was first described in 1939. Anatomically it is characterized by cystic dilatation of ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Medulloblastoma | While leukemias are the most common type of malignancy affecting the pediatric population, brain tumors are the most common solid tumors in this popul ... Read the Article | 1.5 | 17 | Activity DO |
| Medulloblastoma | While leukemias are the most common type of malignancy affecting the pediatric population, brain tumors are the most common solid tumors in this popul ... Read the Article | 1.5 | 17 | Activity MD/PA |
| Melanotic Neuroectodermal Tumor Of Infancy | Melanotic neuroectodermal tumor of infancy (MNTI) is a rapidly growing benign tumor arising from the neural crest cells. It typically affects infants ... Read the Article | 1 | 5 | Activity DO |
| Melanotic Neuroectodermal Tumor Of Infancy | Melanotic neuroectodermal tumor of infancy (MNTI) is a rapidly growing benign tumor arising from the neural crest cells. It typically affects infants ... Read the Article | 1 | 5 | 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 |
| 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 |
| Mesenteric Vasculitis | Mesenteric vasculitis can present in a variety of vasculitic disorders and some systemic, systemic diseases. The diagnosis of this condition can be ve ... Read the Article | 1 | 6 | Activity DO |
| Mesenteric Vasculitis | Mesenteric vasculitis can present in a variety of vasculitic disorders and some systemic, systemic diseases. The diagnosis of this condition can be ve ... Read the Article | 1 | 6 | Activity MD/PA |
| Metachromatic Leukodystrophy | Metachromatic leukodystrophy is a rare lysosomal storage disease caused due to deficient activity of arylsulfatase A. It follows an autosomal recessiv ... Read the Article | 1.25 | 8 | Activity DO |
| Metachromatic Leukodystrophy | Metachromatic leukodystrophy is a rare lysosomal storage disease caused due to deficient activity of arylsulfatase A. It follows an autosomal recessiv ... Read the Article | 1.25 | 8 | 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 |
| Microphthalmia With Cyst | Microphthalmia with cyst is a common, complicated, congenital anomaly whose management is extremely challenging. To avoid significant morbidity and to ... Read the Article | 1 | 5 | Activity DO |
| Microphthalmia With Cyst | Microphthalmia with cyst is a common, complicated, congenital anomaly whose management is extremely challenging. To avoid significant morbidity and to ... Read the Article | 1 | 5 | Activity MD/PA |
| Middle Ear Cholesteatoma | There are two major types of middle ear cholesteatomas, congenital and acquired. Congenital cholesteatomas are derived from remnants of epithelium tha ... Read the Article | 1 | 6 | Activity DO |
| Middle Ear Cholesteatoma | There are two major types of middle ear cholesteatomas, congenital and acquired. Congenital cholesteatomas are derived from remnants of epithelium tha ... Read the Article | 1 | 6 | Activity MD/PA |
| Minimal Change Disease | Minimal change disease (MCD), is one of the most common causes of idiopathic nephrotic syndrome in children. In the past, MCD was given the labels "ni ... Read the Article | 1.25 | 10 | Activity DO |
| Minimal Change Disease | Minimal change disease (MCD), is one of the most common causes of idiopathic nephrotic syndrome in children. In the past, MCD was given the labels "ni ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Mucopolysaccharidosis Type II | Mucopolysaccharidosis Type II (Hunter syndrome) is a rare X-linked recessive disorder. It has an early age of onset with clinical symptoms involving m ... Read the Article | 1.25 | 8 | Activity DO |
| Mucopolysaccharidosis Type II | Mucopolysaccharidosis Type II (Hunter syndrome) is a rare X-linked recessive disorder. It has an early age of onset with clinical symptoms involving m ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Multiple Endocrine Neoplasias Type 2 | Multiple endocrine neoplasia type 2 (MEN 2) is a hereditary cancer syndrome associated primarily with tumors of the adrenal gland, thyroid and parathy ... Read the Article | 1.25 | 10 | Activity DO |
| Multiple Endocrine Neoplasias Type 2 | Multiple endocrine neoplasia type 2 (MEN 2) is a hereditary cancer syndrome associated primarily with tumors of the adrenal gland, thyroid and parathy ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Multiple Endocrine Neoplasias Type 4 | Multiple endocrine neoplasia type 4 (MEN4) is a rare autosomal dominant endocrine tumor syndrome. The most common tumors seen in this condition involv ... Read the Article | 1 | 5 | Activity DO |
| Multiple Endocrine Neoplasias Type 4 | Multiple endocrine neoplasia type 4 (MEN4) is a rare autosomal dominant endocrine tumor syndrome. The most common tumors seen in this condition involv ... Read the Article | 1 | 5 | Activity MD/PA |
| Mumps | Mumps is a contagious viral illness and at one time was a very common childhood disease. With the implementation of widespread vaccination, the incide ... Read the Article | 1 | 5 | Activity DO |
| Mumps | Mumps is a contagious viral illness and at one time was a very common childhood disease. With the implementation of widespread vaccination, the incide ... Read the Article | 1 | 5 | Activity MD/PA |
| Muscle Contraction Tension Headache | Tension-type headache (TTH) is the most common type of primary headaches. It is also sometimes referred to as muscle contraction headache, stress head ... Read the Article | 1.25 | 10 | Activity DO |
| Muscle Contraction Tension Headache | Tension-type headache (TTH) is the most common type of primary headaches. It is also sometimes referred to as muscle contraction headache, stress head ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Muscular Dystrophy | The term "muscular dystrophy" incorporates an assortment of hereditary disorders that lead to progressive, generalized disease of the muscle prompted ... Read the Article | 1.25 | 6 | Activity DO |
| Muscular Dystrophy | The term "muscular dystrophy" incorporates an assortment of hereditary disorders that lead to progressive, generalized disease of the muscle prompted ... Read the Article | 1.25 | 6 | Activity MD/PA |
| Myeloperoxidase Deficiency | Myeloperoxidase (MPO) is a hemoprotein expressed in azurophilic granules of neutrophils and in the lysosomes of monocytes. The enzyme has strong antib ... Read the Article | 1 | 5 | Activity DO |
| Myeloperoxidase Deficiency | Myeloperoxidase (MPO) is a hemoprotein expressed in azurophilic granules of neutrophils and in the lysosomes of monocytes. The enzyme has strong antib ... Read the Article | 1 | 5 | Activity MD/PA |
| Myotonic Dystrophy | Myotonic dystrophy is a rare progressive disorder that universally presents with weakness. In addition to musculoskeletal weakness, cardiac conduction ... Read the Article | 1.25 | 10 | Activity DO |
| Myotonic Dystrophy | Myotonic dystrophy is a rare progressive disorder that universally presents with weakness. In addition to musculoskeletal weakness, cardiac conduction ... Read the Article | 1.25 | 10 | 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 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 |
| Neuroblastoma | Neuroblastoma (NB) is the most frequently-occurring extracranial childhood tumor. It is classified as an embryonal neuroendocrine tumor, originating f ... Read the Article | 1.5 | 16 | Activity DO |
| Neuroblastoma | Neuroblastoma (NB) is the most frequently-occurring extracranial childhood tumor. It is classified as an embryonal neuroendocrine tumor, originating f ... Read the Article | 1.5 | 16 | Activity MD/PA |
| Neurofibromatosis | Neurofibromatosis is a neurocutaneous disorder characterized by tumors in the nervous system and skin. The most common types of neurofibromatosis are ... Read the Article | 1.25 | 10 | Activity DO |
| Neurofibromatosis | Neurofibromatosis is a neurocutaneous disorder characterized by tumors in the nervous system and skin. The most common types of neurofibromatosis are ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Neurofibromatosis Type 1 | Neurofibromatosis-1 (NF-1) or Von Recklinghausen disease is one of the inheritable neurocutaneous disorders manifested by developmental changes in the ... Read the Article | 1.25 | 10 | Activity DO |
| Neurofibromatosis Type 1 | Neurofibromatosis-1 (NF-1) or Von Recklinghausen disease is one of the inheritable neurocutaneous disorders manifested by developmental changes in the ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Neutrophilia | Neutrophilia is defined as a higher neutrophil count in the blood than the normal reference range of absolute neutrophil count. Neutrophilia can be se ... Read the Article | 1 | 7 | Activity DO |
| Neutrophilia | Neutrophilia is defined as a higher neutrophil count in the blood than the normal reference range of absolute neutrophil count. Neutrophilia can be se ... Read the Article | 1 | 7 | Activity MD/PA |
| Nevus Comedonicus | Proper diagnosis and management of nevus comedonicus can lead to better patient outcomes and quality of life. This activity reviews the evaluation, ... Read the Article | 1 | 6 | Activity DO |
| Nevus Comedonicus | Proper diagnosis and management of nevus comedonicus can lead to better patient outcomes and quality of life. This activity reviews the evaluation, ... Read the Article | 1 | 6 | Activity MD/PA |
| Nevus Flammeus | Nevus flammeus or port-wine stain is a capillary malformation usually presenting as a unilateral pink or red patch anywhere on the body of a newborn. ... Read the Article | 1.25 | 7 | Activity DO |
| Nevus Flammeus | Nevus flammeus or port-wine stain is a capillary malformation usually presenting as a unilateral pink or red patch anywhere on the body of a newborn. ... Read the Article | 1.25 | 7 | Activity MD/PA |
| Nevus Of Ota And Ito | Ocular dermal melanosis, also known as nevus of Ota or oculodermal melanocyte, is benign melanosis that involves the distribution of the trigeminal ne ... Read the Article | 1.25 | 12 | Activity DO |
| Nevus Of Ota And Ito | Ocular dermal melanosis, also known as nevus of Ota or oculodermal melanocyte, is benign melanosis that involves the distribution of the trigeminal ne ... Read the Article | 1.25 | 12 | Activity MD/PA |
| Nevus Sebaceus | Nevus sebaceus of Jadassohn also referred to as organoid nevus, is a congenital malformation involving hamartomas of the pilosebaceous follicular unit ... Read the Article | 1 | 7 | Activity DO |
| Nevus Sebaceus | Nevus sebaceus of Jadassohn also referred to as organoid nevus, is a congenital malformation involving hamartomas of the pilosebaceous follicular unit ... Read the Article | 1 | 7 | 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 |
| Non-Hodgkin Lymphoma | Non-Hodgkin lymphoma is a group of malignant neoplasms originating from the lymphoid tissues, mainly the lymph nodes. These tumors may result due to c ... Read the Article | 1.5 | 12 | Activity DO |
| Non-Hodgkin Lymphoma | Non-Hodgkin lymphoma is a group of malignant neoplasms originating from the lymphoid tissues, mainly the lymph nodes. These tumors may result due to c ... Read the Article | 1.5 | 12 | 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 |
| Nonseminomatous Testicular Tumors | Testicular non-seminomatous giant cell tumor (NSGCT) is curable cancer. It can be managed ideally if the medical health providers know the knowledge o ... Read the Article | 1.25 | 5 | Activity DO |
| Nonseminomatous Testicular Tumors | Testicular non-seminomatous giant cell tumor (NSGCT) is curable cancer. It can be managed ideally if the medical health providers know the knowledge o ... Read the Article | 1.25 | 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 |
| Obesity | Obesity is the excessive or abnormal accumulation of fat or adipose tissue in the body that may impair health. Obesity has become an epidemic which ha ... Read the Article | 1.5 | 19 | Activity DO |
| Obesity | Obesity is the excessive or abnormal accumulation of fat or adipose tissue in the body that may impair health. Obesity has become an epidemic which ha ... Read the Article | 1.5 | 19 | Activity MD/PA |
| Obesity Effects On Child Health | Obesity in childhood is the most challenging public health issue in the twenty-first century. Childhood obesity is associated with increased morbidit ... Read the Article | 1 | 5 | Activity DO |
| Obesity Effects On Child Health | Obesity in childhood is the most challenging public health issue in the twenty-first century. Childhood obesity is associated with increased morbidit ... Read the Article | 1 | 5 | Activity MD/PA |
| Obstructive Sleep Apnea | Obstructive sleep apnea (OSA) is characterized by episodes of complete collapse of the airway or partial collapse with an associated decrease in oxyge ... Read the Article | 1.75 | 24 | Activity DO |
| Obstructive Sleep Apnea | Obstructive sleep apnea (OSA) is characterized by episodes of complete collapse of the airway or partial collapse with an associated decrease in oxyge ... Read the Article | 1.75 | 24 | Activity MD/PA |
| Oligodendroglioma | Oligodendroglioma (OG) is a type of diffusely infiltrating glioma and constitutes approximately 5% of primary intracranial tumors. They often involve ... Read the Article | 1.25 | 7 | Activity DO |
| Oligodendroglioma | Oligodendroglioma (OG) is a type of diffusely infiltrating glioma and constitutes approximately 5% of primary intracranial tumors. They often involve ... Read the Article | 1.25 | 7 | 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 |
| Optic Nerve Glioma | Optic pathway gliomas are benign CNS tumors that primarily affect children. Although typically slow growing, the location of these tumors makes resect ... Read the Article | 1 | 5 | Activity DO |
| Optic Nerve Glioma | Optic pathway gliomas are benign CNS tumors that primarily affect children. Although typically slow growing, the location of these tumors makes resect ... Read the Article | 1 | 5 | Activity MD/PA |
| Oral Hemangiomas | Oral hemangiomas are benign tumors that develop in and around the oral cavity due to endothelial cell proliferation. The majority of oral hemangiomas ... Read the Article | 1 | 5 | Activity DO |
| Oral Hemangiomas | Oral hemangiomas are benign tumors that develop in and around the oral cavity due to endothelial cell proliferation. The majority of oral hemangiomas ... 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 |
| Orthostatic Proteinuria | Orthostatic proteinuria, also known as postural proteinuria, is a condition where an abnormally large amount of protein is excreted in the urine when ... Read the Article | 1 | 5 | Activity DO |
| Orthostatic Proteinuria | Orthostatic proteinuria, also known as postural proteinuria, is a condition where an abnormally large amount of protein is excreted in the urine when ... Read the Article | 1 | 5 | Activity MD/PA |
| Osler-Weber-Rendu Disease | Hereditary hemorrhagic telangiectasia (HHT) is also known as Osler–Weber–Rendu disease. It is an autosomal dominant disorder characterized by multiple ... Read the Article | 1 | 8 | Activity DO |
| Osler-Weber-Rendu Disease | Hereditary hemorrhagic telangiectasia (HHT) is also known as Osler–Weber–Rendu disease. It is an autosomal dominant disorder characterized by multiple ... Read the Article | 1 | 8 | Activity MD/PA |
| Osteofibrous Dysplasia | Osteofibrous dysplasia (OFD) is a rare disease. It is considered a benign non-neoplastic condition of unknown cause, characterized by a fibrovascular ... Read the Article | 1 | 6 | Activity DO |
| Osteofibrous Dysplasia | Osteofibrous dysplasia (OFD) is a rare disease. It is considered a benign non-neoplastic condition of unknown cause, characterized by a fibrovascular ... Read the Article | 1 | 6 | 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 |
| Osteomyelitis | Osteomyelitis is a serious infection of the bone that can be either acute or chronic. It is an inflammatory process involving the bone and its structu ... Read the Article | 2 | 24 | Activity DO |
| Osteomyelitis | Osteomyelitis is a serious infection of the bone that can be either acute or chronic. It is an inflammatory process involving the bone and its structu ... Read the Article | 2 | 24 | Activity MD/PA |
| Osteosarcoma | Osteosarcoma is a malignant osseous neoplasm. It is the most common primary bone cancer of childhood. Less frequently, it occurs in adults where it re ... Read the Article | 1.75 | 18 | Activity DO |
| Osteosarcoma | Osteosarcoma is a malignant osseous neoplasm. It is the most common primary bone cancer of childhood. Less frequently, it occurs in adults where it re ... Read the Article | 1.75 | 18 | Activity MD/PA |
| Overview On Ordering and Evaluation of Laboratory Tests | The laboratory medicine service in a hospital is concerned with relevant investigations of patient’s presenting complaints and sometimes with detectio ... Read the Article | 2 | 24 | Activity DO |
| Overview On Ordering and Evaluation of Laboratory Tests | The laboratory medicine service in a hospital is concerned with relevant investigations of patient’s presenting complaints and sometimes with detectio ... Read the Article | 2 | 24 | Activity MD/PA |
| Pancreatic Cysts | Pancreatic cysts are often detected in patients undergoing imaging with either computed tomography (CT) or magnetic resonance imaging (MRI) for unrela ... Read the Article | 1.25 | 9 | Activity DO |
| Pancreatic Cysts | Pancreatic cysts are often detected in patients undergoing imaging with either computed tomography (CT) or magnetic resonance imaging (MRI) for unrela ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Parainfluenza Virus | The human parainfluenza virus (HPIV) is an enveloped, negative-sense, single-stranded RNA virus that belongs to the family of Paramyxoviridae. HPIV ca ... Read the Article | 1.25 | 7 | Activity DO |
| Parainfluenza Virus | The human parainfluenza virus (HPIV) is an enveloped, negative-sense, single-stranded RNA virus that belongs to the family of Paramyxoviridae. HPIV ca ... Read the Article | 1.25 | 7 | 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 |
| 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 | 4 | 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 | 4 | 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 |
| Pediatric Craniopharyngioma | Pediatric craniopharyngioma could be considered one of the most complex neurosurgical pathologies in the pediatric population. The tumor's proximity t ... Read the Article | 1 | 5 | Activity DO |
| Pediatric Craniopharyngioma | Pediatric craniopharyngioma could be considered one of the most complex neurosurgical pathologies in the pediatric population. The tumor's proximity t ... Read the Article | 1 | 5 | Activity MD/PA |
| Pediatric Malignant Pleural Effusion | The pleural cavity is a thin layer of the sac that is lined with a serous membrane that encloses the lungs and separates it from the thoracic cage. Th ... Read the Article | 1 | 4 | Activity DO |
| Pediatric Malignant Pleural Effusion | The pleural cavity is a thin layer of the sac that is lined with a serous membrane that encloses the lungs and separates it from the thoracic cage. Th ... Read the Article | 1 | 4 | Activity MD/PA |
| Pelizaeus-Merzbacher Disease | Pelizaeus-Merzbacher disease (PMD) is a demyelinating disorder of the CNS belonging to the group of hypomyelination leukodystrophies. This activity de ... Read the Article | 1 | 5 | Activity DO |
| Pelizaeus-Merzbacher Disease | Pelizaeus-Merzbacher disease (PMD) is a demyelinating disorder of the CNS belonging to the group of hypomyelination leukodystrophies. This activity de ... Read the Article | 1 | 5 | 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 |
| 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 |
| Phenol Toxicity | Phenol is a historical disinfectant with continued use in industry, laboratories, and some health care settings. Phenol is a protoplasmic poison that ... Read the Article | 1 | 5 | Activity DO |
| Phenol Toxicity | Phenol is a historical disinfectant with continued use in industry, laboratories, and some health care settings. Phenol is a protoplasmic poison that ... Read the Article | 1 | 5 | 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 |
| Piebaldism | Piebaldism is an autosomal dominant disorder of melanocyte migration and development characterized by isolated congenital leukoderma (white skin) and ... Read the Article | 1 | 4 | Activity DO |
| Piebaldism | Piebaldism is an autosomal dominant disorder of melanocyte migration and development characterized by isolated congenital leukoderma (white skin) and ... Read the Article | 1 | 4 | 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 |
| Pilocytic Astrocytoma | Pilocytic astrocytoma is the most common childhood brain tumor and most often found in the posterior fossa. Complete resection usually cures the patie ... Read the Article | 1.25 | 8 | Activity DO |
| Pilocytic Astrocytoma | Pilocytic astrocytoma is the most common childhood brain tumor and most often found in the posterior fossa. Complete resection usually cures the patie ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Pineal Gland Cancer | Tumors of the pineal region are rare and account for 1% of all intracranial tumors in adults and up to 8% in children. Multiple pathologies are associ ... Read the Article | 1.25 | 7 | Activity DO |
| Pineal Gland Cancer | Tumors of the pineal region are rare and account for 1% of all intracranial tumors in adults and up to 8% in children. Multiple pathologies are associ ... Read the Article | 1.25 | 7 | Activity MD/PA |
| Pleuropulmonary Blastoma | Pleuropulmonary blastomas are rare, malignant mesenchymal tumors that typically present with non-specific symptoms. Radiologic features may increase t ... Read the Article | 1 | 4 | Activity DO |
| Pleuropulmonary Blastoma | Pleuropulmonary blastomas are rare, malignant mesenchymal tumors that typically present with non-specific symptoms. Radiologic features may increase t ... Read the Article | 1 | 4 | Activity MD/PA |
| Polycystic Kidney Disease | Polycystic kidney disease (ADPKD) is an autosomal dominant disorder. It is a multisystem and progressive disease with cysts formation and kidney enlar ... Read the Article | 1.25 | 12 | Activity DO |
| Polycystic Kidney Disease | Polycystic kidney disease (ADPKD) is an autosomal dominant disorder. It is a multisystem and progressive disease with cysts formation and kidney enlar ... Read the Article | 1.25 | 12 | 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 |
| Pott Puffy Tumor | Pott puffy tumor is a subperiosteal abscess due to associated frontal skull osteomyelitis. This usually occurs as a rare complication of frontal sinus ... Read the Article | 1 | 5 | Activity DO |
| Pott Puffy Tumor | Pott puffy tumor is a subperiosteal abscess due to associated frontal skull osteomyelitis. This usually occurs as a rare complication of frontal sinus ... Read the Article | 1 | 5 | 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 |
| Precocious Pseudopuberty | Precocious puberty is traditionally defined as the appearance of secondary sexual characteristics before the age of eight years in girls and nine year ... Read the Article | 1 | 5 | Activity DO |
| Precocious Pseudopuberty | Precocious puberty is traditionally defined as the appearance of secondary sexual characteristics before the age of eight years in girls and nine year ... Read the Article | 1 | 5 | Activity MD/PA |
| Primary Bone Cancer | Primary bone cancers are rare malignant tumors originating in bone and derived from primitive mesenchymal cells. They are frequently aggressive tumors ... Read the Article | 1.25 | 10 | Activity DO |
| Primary Bone Cancer | Primary bone cancers are rare malignant tumors originating in bone and derived from primitive mesenchymal cells. They are frequently aggressive tumors ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Primary Lung Tuberculosis | Tuberculosis is the leading cause of death from an infectious agent worldwide, causing even more deaths in HIV/AIDS patients. A third of the world's p ... Read the Article | 1.25 | 11 | Activity DO |
| Primary Lung Tuberculosis | Tuberculosis is the leading cause of death from an infectious agent worldwide, causing even more deaths in HIV/AIDS patients. A third of the world's p ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Primitive Neuroectodermal Tumor | In 2016, the World Health Organization published a revised classification of central nervous system tumors using molecular parameters. In this classif ... Read the Article | 1 | 5 | Activity DO |
| Primitive Neuroectodermal Tumor | In 2016, the World Health Organization published a revised classification of central nervous system tumors using molecular parameters. In this classif ... Read the Article | 1 | 5 | 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 |
| 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 |
| Pyruvate Kinase Deficiency | Pyruvate kinase deficiency (PKD) is the most common enzyme-related glycolytic defect that results in red cell hemolysis. Invariably, PKD results in he ... Read the Article | 1.25 | 9 | Activity DO |
| Pyruvate Kinase Deficiency | Pyruvate kinase deficiency (PKD) is the most common enzyme-related glycolytic defect that results in red cell hemolysis. Invariably, PKD results in he ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Radial Dysplasia | The radial club hand encompasses a spectrum of complex congenital malformations of the radial side of the forearm. These are uncommon and can range fr ... Read the Article | 1 | 6 | Activity DO |
| Radial Dysplasia | The radial club hand encompasses a spectrum of complex congenital malformations of the radial side of the forearm. These are uncommon and can range fr ... Read the Article | 1 | 6 | Activity MD/PA |
| Rat-bite Fever | Rat-bite fever, also known as streptobacillosis, spirillary fever, bogger, and epidemic arthritic erythema, is a zoonotic illness that manifests with ... Read the Article | 1 | 6 | Activity DO |
| Rat-bite Fever | Rat-bite fever, also known as streptobacillosis, spirillary fever, bogger, and epidemic arthritic erythema, is a zoonotic illness that manifests with ... Read the Article | 1 | 6 | Activity MD/PA |
| Refsum Disease | Refsum disease is a rare autosomal recessive disease from the peroxisomal biogenesis spectrum of disorders. Peroxisomes are multiple membrane-bound in ... Read the Article | 1 | 6 | Activity DO |
| Refsum Disease | Refsum disease is a rare autosomal recessive disease from the peroxisomal biogenesis spectrum of disorders. Peroxisomes are multiple membrane-bound in ... Read the Article | 1 | 6 | 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 |
| Renal Tubular Acidosis | Kidneys play a pivotal role in maintaining the acid-base balance of body along with lungs, and they do so by reabsorbing filtered bicarbonate and remo ... Read the Article | 1.25 | 12 | Activity DO |
| Renal Tubular Acidosis | Kidneys play a pivotal role in maintaining the acid-base balance of body along with lungs, and they do so by reabsorbing filtered bicarbonate and remo ... Read the Article | 1.25 | 12 | Activity MD/PA |
| Retinoblastoma | Retinoblastoma is the most common primary intraocular malignancy of childhood. Patients management is best in consultation with an experienced ophthal ... Read the Article | 1.25 | 10 | Activity DO |
| Retinoblastoma | Retinoblastoma is the most common primary intraocular malignancy of childhood. Patients management is best in consultation with an experienced ophthal ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Rhabdomyosarcoma | Rhabdomyosarcoma (RMS) is a primitive pediatric malignant soft tissue sarcoma of skeletal muscle phenotype that originates from a primitive mesenchyma ... Read the Article | 1.25 | 12 | Activity DO |
| Rhabdomyosarcoma | Rhabdomyosarcoma (RMS) is a primitive pediatric malignant soft tissue sarcoma of skeletal muscle phenotype that originates from a primitive mesenchyma ... Read the Article | 1.25 | 12 | Activity MD/PA |
| Rheumatic Heart Disease | Rheumatic heart disease is a systemic immune condition that occurs as a complication of rheumatic fever. This occurs after a beta-hemolytic streptococ ... Read the Article | 1.5 | 17 | Activity DO |
| Rheumatic Heart Disease | Rheumatic heart disease is a systemic immune condition that occurs as a complication of rheumatic fever. This occurs after a beta-hemolytic streptococ ... Read the Article | 1.5 | 17 | 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 |
| Rickets | Rickets is a condition characterized by a defect in mineralization of the epiphyseal plates. Rickets could be inherited or acquired. The acquired rick ... Read the Article | 1.25 | 11 | Activity DO |
| Rickets | Rickets is a condition characterized by a defect in mineralization of the epiphyseal plates. Rickets could be inherited or acquired. The acquired rick ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Rickettsial Infection | Rickettsia is a group of vector-borne organisms that cause acute febrile illnesses throughout the world. While the clinical presentation of rickettsia ... Read the Article | 1 | 7 | Activity DO |
| Rickettsial Infection | Rickettsia is a group of vector-borne organisms that cause acute febrile illnesses throughout the world. While the clinical presentation of rickettsia ... Read the Article | 1 | 7 | Activity MD/PA |
| Rotor Syndrome | Rotors syndrome, also known as Rotor type hyperbilirubinemia, is an autosomal recessive disease and a rare cause of mixed direct (conjugated) and indi ... Read the Article | 1 | 7 | Activity DO |
| Rotor Syndrome | Rotors syndrome, also known as Rotor type hyperbilirubinemia, is an autosomal recessive disease and a rare cause of mixed direct (conjugated) and indi ... Read the Article | 1 | 7 | Activity MD/PA |
| Rubeola (Measles) | This activity reviews the epidemiology and pathophysiology of measles to further understand its epidemiological situation. This will hopefully lead to ... Read the Article | 1.5 | 13 | Activity DO |
| Rubeola (Measles) | This activity reviews the epidemiology and pathophysiology of measles to further understand its epidemiological situation. This will hopefully lead to ... Read the Article | 1.5 | 13 | Activity MD/PA |
| Scaphocephaly | Scaphocephaly is the term used to describe the narrow and long abnormal skull shape in sagittal craniosynostosis due to the premature fusion of the sa ... Read the Article | 1 | 5 | Activity DO |
| Scaphocephaly | Scaphocephaly is the term used to describe the narrow and long abnormal skull shape in sagittal craniosynostosis due to the premature fusion of the sa ... Read the Article | 1 | 5 | Activity MD/PA |
| Schizencephaly | Schizencephaly is a rare congenital neuronal migration disorder characterized by cleft lined by the heterotopic gray matter, which connects the surfac ... Read the Article | 1 | 7 | Activity DO |
| Schizencephaly | Schizencephaly is a rare congenital neuronal migration disorder characterized by cleft lined by the heterotopic gray matter, which connects the surfac ... Read the Article | 1 | 7 | Activity MD/PA |
| Serum Sickness | Serum sickness is a rare but important cause of fever, arthritis, and rash in both children and adults. This activity reviews the differences between ... Read the Article | 1 | 5 | Activity DO |
| Serum Sickness | Serum sickness is a rare but important cause of fever, arthritis, and rash in both children and adults. This activity reviews the differences between ... Read the Article | 1 | 5 | Activity MD/PA |
| Shwachman-Diamond Syndrome | Schwachman-Diamond syndrome (SDS) is an autosomal recessive disorder that is the second most common cause of exocrine pancreatic insufficiency after c ... Read the Article | 1 | 4 | Activity DO |
| Shwachman-Diamond Syndrome | Schwachman-Diamond syndrome (SDS) is an autosomal recessive disorder that is the second most common cause of exocrine pancreatic insufficiency after c ... Read the Article | 1 | 4 | 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 | 1.75 | 20 | 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 | 1.75 | 20 | Activity MD/PA |
| Sonography Pediatric Gynecology Assessment, Protocols, And Interpretation | Female pediatric and adolescent patients can present with numerous genital pathologies, including congenital, infectious, masses, or syndromic associa ... Read the Article | 1 | 5 | Activity DO |
| Sonography Pediatric Gynecology Assessment, Protocols, And Interpretation | Female pediatric and adolescent patients can present with numerous genital pathologies, including congenital, infectious, masses, or syndromic associa ... Read the Article | 1 | 5 | Activity MD/PA |
| Spinal Cord Abscess | Intramedullary spinal cord abscess (ISCA) is a rare central nervous system infection associated with high mortality and neurological morbidity. A qui ... Read the Article | 1 | 5 | Activity DO |
| Spinal Cord Abscess | Intramedullary spinal cord abscess (ISCA) is a rare central nervous system infection associated with high mortality and neurological morbidity. A qui ... Read the Article | 1 | 5 | 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 | 11 | 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 | 11 | Activity MD/PA |
| Spinal Metastasis | Spinal metastases are the most common tumors of the spine. These are more commonly found as bone metastasis and may present with symptoms of spinal ca ... Read the Article | 1.25 | 12 | Activity DO |
| Spinal Metastasis | Spinal metastases are the most common tumors of the spine. These are more commonly found as bone metastasis and may present with symptoms of spinal ca ... Read the Article | 1.25 | 12 | Activity MD/PA |
| Steatorrhea | The management of steatorrhea is complex and new approaches have been introduced. To achieve satisfactory outcomes, the basic and clinical aspects of ... Read the Article | 1 | 6 | Activity DO |
| Steatorrhea | The management of steatorrhea is complex and new approaches have been introduced. To achieve satisfactory outcomes, the basic and clinical aspects of ... Read the Article | 1 | 6 | 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 |
| 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 |
| Subacute Necrotizing Encephalomyelopathy | Subacute necrotizing encephalomyelopathy (SNE) is primarily a disease of childhood that affects the central nervous system. This is a rare condition t ... Read the Article | 1.25 | 11 | Activity DO |
| Subacute Necrotizing Encephalomyelopathy | Subacute necrotizing encephalomyelopathy (SNE) is primarily a disease of childhood that affects the central nervous system. This is a rare condition t ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Subacute Sclerosing Panencephalitis | Subacute sclerosing panencephalitis (SSPE) is a devastating complication of the measles virus. Although it is a rare complication and the measles viru ... Read the Article | 1 | 5 | Activity DO |
| Subacute Sclerosing Panencephalitis | Subacute sclerosing panencephalitis (SSPE) is a devastating complication of the measles virus. Although it is a rare complication and the measles viru ... Read the Article | 1 | 5 | 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 |
| Syndactyly | Syndactyly is one of the most common congenital anomalies of the extremities. It is a failure of differentiation of the digits, defined as a fusion of ... Read the Article | 1 | 6 | Activity DO |
| Syndactyly | Syndactyly is one of the most common congenital anomalies of the extremities. It is a failure of differentiation of the digits, defined as a fusion of ... Read the Article | 1 | 6 | Activity MD/PA |
| Testicular Teratoma | Testicular teratoma is a neoplasm derived from germ cells of the testicle. It can display diverse biological behavior with an aggressive nature at tim ... Read the Article | 1.25 | 7 | Activity DO |
| Testicular Teratoma | Testicular teratoma is a neoplasm derived from germ cells of the testicle. It can display diverse biological behavior with an aggressive nature at tim ... Read the Article | 1.25 | 7 | Activity MD/PA |
| Testicular Torsion | Scrotal complaints are relatively common both in primary care and in the emergency department and comprise at least 0.5 percent of all emergency depar ... Read the Article | 1.5 | 18 | Activity DO |
| Testicular Torsion | Scrotal complaints are relatively common both in primary care and in the emergency department and comprise at least 0.5 percent of all emergency depar ... Read the Article | 1.5 | 18 | 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 |
| Tetralogy of Fallot | Tetralogy of Fallot is a congenital anomaly resulting in pulmonary stenosis, an interventricular defect, biventricular aortal origin, and right ventri ... Read the Article | 1.5 | 15 | Activity DO |
| Tetralogy of Fallot | Tetralogy of Fallot is a congenital anomaly resulting in pulmonary stenosis, an interventricular defect, biventricular aortal origin, and right ventri ... Read the Article | 1.5 | 15 | Activity MD/PA |
| Tinea Versicolor | Pityriasis versicolor, also known as tinea versicolor, is a common, benign, superficial fungal infection of the skin. Clinical features of pityriasis ... Read the Article | 1 | 8 | Activity DO |
| Tinea Versicolor | Pityriasis versicolor, also known as tinea versicolor, is a common, benign, superficial fungal infection of the skin. Clinical features of pityriasis ... Read the Article | 1 | 8 | 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 |
| Total Parenteral Nutrition | Total parenteral nutrition is a medication used in the management and treatment of malnourishment. It is in the nutrition class of drugs. This activit ... Read the Article | 1.75 | 21 | Activity DO |
| Total Parenteral Nutrition | Total parenteral nutrition is a medication used in the management and treatment of malnourishment. It is in the nutrition class of drugs. This activit ... Read the Article | 1.75 | 21 | Activity MD/PA |
| Totalis Alopecia | Alopecia totalis is a chronic condition of complete hair loss of the scalp, which affects a small percentage of patients with alopecia areata. Treatme ... Read the Article | 1 | 5 | Activity DO |
| Totalis Alopecia | Alopecia totalis is a chronic condition of complete hair loss of the scalp, which affects a small percentage of patients with alopecia areata. Treatme ... Read the Article | 1 | 5 | Activity MD/PA |
| Toxocara Canis | Human toxocariasis is a helminth infection that primarily impacts individuals of lower socioeconomic class in tropical and subtropical regions around ... Read the Article | 1 | 5 | Activity DO |
| Toxocara Canis | Human toxocariasis is a helminth infection that primarily impacts individuals of lower socioeconomic class in tropical and subtropical regions around ... Read the Article | 1 | 5 | Activity MD/PA |
| Transient Hypogammaglobulinemia of Infancy | Transient hypogammaglobulinemia of infancy (THI) is a type of antibody deficiency that affects infant and children typically below the age of 6 years. ... Read the Article | 1 | 4 | Activity DO |
| Transient Hypogammaglobulinemia of Infancy | Transient hypogammaglobulinemia of infancy (THI) is a type of antibody deficiency that affects infant and children typically below the age of 6 years. ... Read the Article | 1 | 4 | Activity MD/PA |
| Trigonocephaly | Trigonocephaly is the premature closure of the metopic suture forming a triangular forehead, with an obvious or subtle osseous ridge. This activity re ... Read the Article | 1 | 5 | Activity DO |
| Trigonocephaly | Trigonocephaly is the premature closure of the metopic suture forming a triangular forehead, with an obvious or subtle osseous ridge. This activity re ... Read the Article | 1 | 5 | Activity MD/PA |
| Trinucleotide Repeat Disorders | Trinucleotide repeat disorders are neuropsychiatric disorders caused due to abnormal trinucleotide repeat expansions. Accurate diagnosis, with knowled ... Read the Article | 1 | 5 | Activity DO |
| Trinucleotide Repeat Disorders | Trinucleotide repeat disorders are neuropsychiatric disorders caused due to abnormal trinucleotide repeat expansions. Accurate diagnosis, with knowled ... Read the Article | 1 | 5 | 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 | 9 | 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 | 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 |
| 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 |
| 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 |
| Velocardiofacial Syndrome | Velocardiofacial syndrome, also known as Di George syndrome or chromosome 22q11.2 syndrome, is the most common microdeletion syndrome in humans. Thoug ... Read the Article | 1 | 4 | Activity DO |
| Velocardiofacial Syndrome | Velocardiofacial syndrome, also known as Di George syndrome or chromosome 22q11.2 syndrome, is the most common microdeletion syndrome in humans. Thoug ... Read the Article | 1 | 4 | 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 | 1.25 | 12 | 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 | 1.25 | 12 | Activity MD/PA |
| Vesicoureteral Reflux | Retrograde urine flow from the bladder to the upper urinary tract is known as vesicoureteric reflux. This article illustrates the anatomy and pathophy ... Read the Article | 1 | 6 | Activity DO |
| Vesicoureteral Reflux | Retrograde urine flow from the bladder to the upper urinary tract is known as vesicoureteric reflux. This article illustrates the anatomy and pathophy ... Read the Article | 1 | 6 | Activity MD/PA |
| Vitamin D Deficiency | Vitamin D is a fat-soluble vitamin used by the body for normal bone development and maintenance by increasing the absorption of calcium, magnesium, an ... Read the Article | 1.25 | 11 | Activity DO |
| Vitamin D Deficiency | Vitamin D is a fat-soluble vitamin used by the body for normal bone development and maintenance by increasing the absorption of calcium, magnesium, an ... Read the Article | 1.25 | 11 | 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 |
| Waterhouse-Friderichsen Syndrome | Waterhouse Friderichsen syndrome is a rare but life-threatening disorder associated with bilateral adrenal hemorrhage. In many cases, it is caused by ... Read the Article | 1 | 5 | Activity DO |
| Waterhouse-Friderichsen Syndrome | Waterhouse Friderichsen syndrome is a rare but life-threatening disorder associated with bilateral adrenal hemorrhage. In many cases, it is caused by ... Read the Article | 1 | 5 | 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 |
| Wilms Tumor | Wilms tumor, or nephroblastoma, is the most common pediatric renal cancer, the most common pediatric abdominal cancer, and the fourth most common pedi ... Read the Article | 1.5 | 13 | Activity DO |
| Wilms Tumor | Wilms tumor, or nephroblastoma, is the most common pediatric renal cancer, the most common pediatric abdominal cancer, and the fourth most common pedi ... Read the Article | 1.5 | 13 | Activity MD/PA |
| Wiskott-Aldrich Syndrome | Wiskott-Aldrich syndrome (WAS) is a rare X-linked disorder which classically includes the characteristic triad of immunodeficiency, thrombocytopenia, ... Read the Article | 1.25 | 13 | Activity DO |
| Wiskott-Aldrich Syndrome | Wiskott-Aldrich syndrome (WAS) is a rare X-linked disorder which classically includes the characteristic triad of immunodeficiency, thrombocytopenia, ... Read the Article | 1.25 | 13 | Activity MD/PA |
| X-linked Agammaglobulinemia | X-linked agammaglobulinemia or XLA is a primary immunodeficiency disorder that prevents affected individuals from making antibodies and requires them ... Read the Article | 1 | 5 | Activity DO |
| X-linked Agammaglobulinemia | X-linked agammaglobulinemia or XLA is a primary immunodeficiency disorder that prevents affected individuals from making antibodies and requires them ... Read the Article | 1 | 5 | 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 |
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