Pediatric-Developmental CME
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Pediatric-Developmental Articles (198)
Featured Activities
Pediatric-Developmental Activities
| Title | Description | Hours | Questions | |
|---|---|---|---|---|
| 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 |
| Absence Seizure | Absence seizures are brief seizures during which the patient is unresponsive. They are generally seen in children between 4 and 12 years of age. It ha ... Read the Article | 1.25 | 12 | Activity DO |
| Absence Seizure | Absence seizures are brief seizures during which the patient is unresponsive. They are generally seen in children between 4 and 12 years of age. It ha ... Read the Article | 1.25 | 12 | Activity MD/PA |
| Achondroplasia | Achondroplasia is the most common skeletal dysplasia found in humans, accounting for 90% of cases of disproportionate short stature. It is caused by a ... Read the Article | 1.5 | 13 | Activity DO |
| Achondroplasia | Achondroplasia is the most common skeletal dysplasia found in humans, accounting for 90% of cases of disproportionate short stature. It is caused by a ... Read the Article | 1.5 | 13 | Activity MD/PA |
| Acrodermatitis Enteropathica | Acrodermatitis enteropathica is a rare skin disorder associated with zinc deficiency that is most often seen in infants. Zinc is a very important micr ... Read the Article | 1 | 7 | Activity DO |
| Acrodermatitis Enteropathica | Acrodermatitis enteropathica is a rare skin disorder associated with zinc deficiency that is most often seen in infants. Zinc is a very important micr ... Read the Article | 1 | 7 | Activity MD/PA |
| Adolescent and Idiopathic Scoliosis | Adolescent idiopathic scoliosis (AIS) is the most common form of pediatric scoliosis occurring in individuals between the ages of 10 to 18. By definit ... Read the Article | 1.5 | 14 | Activity DO |
| Adolescent and Idiopathic Scoliosis | Adolescent idiopathic scoliosis (AIS) is the most common form of pediatric scoliosis occurring in individuals between the ages of 10 to 18. By definit ... Read the Article | 1.5 | 14 | 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 |
| Aflatoxin Toxicity | Aflatoxins are metabolites produced by toxigenic strains of molds, mainly Aspergillus flavus and A. parasiticus which grow in soil, hay, decaying vege ... Read the Article | 1 | 5 | Activity DO |
| Aflatoxin Toxicity | Aflatoxins are metabolites produced by toxigenic strains of molds, mainly Aspergillus flavus and A. parasiticus which grow in soil, hay, decaying vege ... Read the Article | 1 | 5 | Activity MD/PA |
| Aggression In Hypothalamic Hamartoma | Psychiatric symptoms are a common comorbid feature of hypothalamic hamartoma with epilepsy. They are most disabling and are a significant challenge fo ... Read the Article | 1 | 5 | Activity DO |
| Aggression In Hypothalamic Hamartoma | Psychiatric symptoms are a common comorbid feature of hypothalamic hamartoma with epilepsy. They are most disabling and are a significant challenge fo ... Read the Article | 1 | 5 | Activity MD/PA |
| Airway Management | Interprofessional team members must be familiar with the important anatomical, physiological, and pathological features related to the airway and have ... Read the Article | 1.75 | 19 | Activity DO |
| Airway Management | Interprofessional team members must be familiar with the important anatomical, physiological, and pathological features related to the airway and have ... Read the Article | 1.75 | 19 | Activity MD/PA |
| Akinesia | Akinesia or "absent movement" is a clinical sign that could be indicative of a number of disorders, depending on the age group of the patient. The var ... Read the Article | 1 | 5 | Activity DO |
| Akinesia | Akinesia or "absent movement" is a clinical sign that could be indicative of a number of disorders, depending on the age group of the patient. The var ... Read the Article | 1 | 5 | Activity MD/PA |
| Alagille Syndrome | Alagille syndrome (ALGS) is a multisystem autosomal dominant disorder with a wide variety of clinical manifestations. It is also known as arteriohepat ... Read the Article | 1 | 6 | Activity DO |
| Alagille Syndrome | Alagille syndrome (ALGS) is a multisystem autosomal dominant disorder with a wide variety of clinical manifestations. It is also known as arteriohepat ... Read the Article | 1 | 6 | Activity MD/PA |
| 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 |
| Alexander Disease | Alexander disease is a relatively rare leukodystrophy that generally presents in the infantile period, although other variants are occasionally seen. ... Read the Article | 1 | 4 | Activity DO |
| Alexander Disease | Alexander disease is a relatively rare leukodystrophy that generally presents in the infantile period, although other variants are occasionally seen. ... Read the Article | 1 | 4 | Activity MD/PA |
| Allgrove Syndrome | Allgrove syndrome (AS) or 3A syndrome (AAA) is characterized by a triad of adrenocorticotrophic hormone (ACTH) resistant adrenal insufficiency, alacri ... Read the Article | 1 | 3 | Activity DO |
| Allgrove Syndrome | Allgrove syndrome (AS) or 3A syndrome (AAA) is characterized by a triad of adrenocorticotrophic hormone (ACTH) resistant adrenal insufficiency, alacri ... Read the Article | 1 | 3 | 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 |
| Amphetamine | Amphetamine is a medication used in the management and treatment of ADHD and narcolepsy. It is classified as a central nervous system stimulant. This ... Read the Article | 1 | 5 | Activity DO |
| Amphetamine | Amphetamine is a medication used in the management and treatment of ADHD and narcolepsy. It is classified as a central nervous system stimulant. This ... Read the Article | 1 | 5 | 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 | 6 | 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 | 6 | Activity MD/PA |
| Angelman Syndrome | Angelman syndrome is a rare disorder caused by loss of function of the maternal UBE3A. It presents in childhood with psychomotor delay, absent speech, ... Read the Article | 1 | 6 | Activity DO |
| Angelman Syndrome | Angelman syndrome is a rare disorder caused by loss of function of the maternal UBE3A. It presents in childhood with psychomotor delay, absent speech, ... Read the Article | 1 | 6 | Activity MD/PA |
| Aortopulmonary Septal Defect | An aortopulmonary or septal defect/aortopulmonary window is one of the rarest congenital heart defects. This defect develops embryologically when ther ... Read the Article | 1 | 7 | Activity DO |
| Aortopulmonary Septal Defect | An aortopulmonary or septal defect/aortopulmonary window is one of the rarest congenital heart defects. This defect develops embryologically when ther ... Read the Article | 1 | 7 | Activity MD/PA |
| Art Therapy | Creative art therapy is a complementary therapy used to assist patients with serious illness to ameliorate symptom burden and adapt to the stressful l ... Read the Article | 1 | 6 | Activity DO |
| Art Therapy | Creative art therapy is a complementary therapy used to assist patients with serious illness to ameliorate symptom burden and adapt to the stressful l ... Read the Article | 1 | 6 | Activity MD/PA |
| Asperger Syndrome | Asperger syndrome is a neurodevelopmental disorder within the large family of autism spectrum disorder. It is characterized by impaired social communi ... Read the Article | 1.25 | 5 | Activity DO |
| Asperger Syndrome | Asperger syndrome is a neurodevelopmental disorder within the large family of autism spectrum disorder. It is characterized by impaired social communi ... Read the Article | 1.25 | 5 | 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 |
| Athetoid Cerebral Palsy | Athetoid cerebral palsy, also known as dyskinetic cerebral palsy, is the second most common subtype of cerebral palsy. It is a non-progressive, perman ... Read the Article | 1 | 5 | Activity DO |
| Athetoid Cerebral Palsy | Athetoid cerebral palsy, also known as dyskinetic cerebral palsy, is the second most common subtype of cerebral palsy. It is a non-progressive, perman ... Read the Article | 1 | 5 | Activity MD/PA |
| Atrioventricular Septal Defect | The atrioventricular septal defect is a congenital cardiac malformation that is characterized by a variable degree of the atrial and ventricular septa ... Read the Article | 1.25 | 11 | Activity DO |
| Atrioventricular Septal Defect | The atrioventricular septal defect is a congenital cardiac malformation that is characterized by a variable degree of the atrial and ventricular septa ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Attention Deficit Hyperactivity Disorder | The diagnosis of attention deficit hyperactivity disorder (ADHD) has been surrounded by controversy over the last century. Over the past 30 years, how ... Read the Article | 1.75 | 21 | Activity DO |
| Attention Deficit Hyperactivity Disorder | The diagnosis of attention deficit hyperactivity disorder (ADHD) has been surrounded by controversy over the last century. Over the past 30 years, how ... Read the Article | 1.75 | 21 | Activity MD/PA |
| Auditory Brainstem Response | Auditory brainstem response helps diagnose suspected neurologic abnormalities of the 8th cranial nerve as well as the associated auditory pathways and ... Read the Article | 1 | 5 | Activity DO |
| Auditory Brainstem Response | Auditory brainstem response helps diagnose suspected neurologic abnormalities of the 8th cranial nerve as well as the associated auditory pathways and ... Read the Article | 1 | 5 | Activity MD/PA |
| Autism Spectrum Disorder | Autism spectrum disorders (ASD) are a group of rapidly growing disabilities. They are characterized by repetitive patterns of behavior, interests, or ... Read the Article | 1.75 | 23 | Activity DO |
| Autism Spectrum Disorder | Autism spectrum disorders (ASD) are a group of rapidly growing disabilities. They are characterized by repetitive patterns of behavior, interests, or ... Read the Article | 1.75 | 23 | 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 |
| Behavior Modification | Behavior modification is a psychotherapeutic intervention primarily used to eliminate or reduce maladaptive behavior in children or adults. While some ... Read the Article | 1.5 | 19 | Activity DO |
| Behavior Modification | Behavior modification is a psychotherapeutic intervention primarily used to eliminate or reduce maladaptive behavior in children or adults. While some ... Read the Article | 1.5 | 19 | 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 |
| C 17 Hydroxylase Deficiency | Congenital adrenal hyperplasia (CAH) covers a group of autosomal recessive disorders caused by a deficiency of one of the enzymes required for the ste ... Read the Article | 1 | 6 | Activity DO |
| C 17 Hydroxylase Deficiency | Congenital adrenal hyperplasia (CAH) covers a group of autosomal recessive disorders caused by a deficiency of one of the enzymes required for the ste ... Read the Article | 1 | 6 | Activity MD/PA |
| Cafe Au Lait Macules | Cafe-au-lait macules (CALMs) are common pigmented lesions found in the general population. They can be described as well-circumscribed, pigmented macu ... Read the Article | 1.25 | 8 | Activity DO |
| Cafe Au Lait Macules | Cafe-au-lait macules (CALMs) are common pigmented lesions found in the general population. They can be described as well-circumscribed, pigmented macu ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Canavan Disease | Canavan disease, also called Canavan-Van Bogaert-Bertrand disease, is a rare, progressive, and fatal neurological hereditary disorder that begins in i ... Read the Article | 1 | 7 | Activity DO |
| Canavan Disease | Canavan disease, also called Canavan-Van Bogaert-Bertrand disease, is a rare, progressive, and fatal neurological hereditary disorder that begins in i ... Read the Article | 1 | 7 | Activity MD/PA |
| Catatonic Schizophrenia | Catatonic schizophrenia is one of the classical clinical subtypes of schizophrenia. The concept of catatonic symptoms in schizophrenia has changed thr ... Read the Article | 1 | 5 | Activity DO |
| Catatonic Schizophrenia | Catatonic schizophrenia is one of the classical clinical subtypes of schizophrenia. The concept of catatonic symptoms in schizophrenia has changed thr ... Read the Article | 1 | 5 | 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 |
| Child Development | The stages through which a child goes through from birth until he or she becomes an adult is child development. Children are first newborns, and durin ... Read the Article | 4.5 | 85 | Activity DO |
| Child Development | The stages through which a child goes through from birth until he or she becomes an adult is child development. Children are first newborns, and durin ... Read the Article | 4.5 | 85 | Activity MD/PA |
| Child Physical Abuse And Neglect | Approximately one in four children experience child abuse or neglect in their lifetime. Of maltreated children, 18 percent are abused physically, 78 p ... Read the Article | 1 | 5 | Activity DO |
| Child Physical Abuse And Neglect | Approximately one in four children experience child abuse or neglect in their lifetime. Of maltreated children, 18 percent are abused physically, 78 p ... Read the Article | 1 | 5 | Activity MD/PA |
| Chromosome Instability Syndromes | Chromosomal instability syndromes are a group of inherited disorders associated with chromosomal instability and breakage either spontaneously or in r ... Read the Article | 1 | 5 | Activity DO |
| Chromosome Instability Syndromes | Chromosomal instability syndromes are a group of inherited disorders associated with chromosomal instability and breakage either spontaneously or in r ... Read the Article | 1 | 5 | 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 |
| Coarctation of the Aorta | Coarctation of the aorta is a narrowing of the aorta, most commonly occurring just beyond the left subclavian artery. However, it can occur in various ... Read the Article | 1.5 | 14 | Activity DO |
| Coarctation of the Aorta | Coarctation of the aorta is a narrowing of the aorta, most commonly occurring just beyond the left subclavian artery. However, it can occur in various ... Read the Article | 1.5 | 14 | Activity MD/PA |
| Cockayne Syndrome | Cockayne syndrome, first described in 1936 by Dr. Cockayne, is a rare genetic disorder, mainly characterized by growth disorders, intellectual deficit ... Read the Article | 1 | 4 | Activity DO |
| Cockayne Syndrome | Cockayne syndrome, first described in 1936 by Dr. Cockayne, is a rare genetic disorder, mainly characterized by growth disorders, intellectual deficit ... Read the Article | 1 | 4 | Activity MD/PA |
| 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 |
| Coprolalia | Coprolalia comes from the greek "kopros," which means "dung, feces" and "lalein," which means "to babble." It's a tic-like occurrence that involves no ... Read the Article | 1 | 7 | Activity DO |
| Coprolalia | Coprolalia comes from the greek "kopros," which means "dung, feces" and "lalein," which means "to babble." It's a tic-like occurrence that involves no ... Read the Article | 1 | 7 | 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 |
| Corpus Callosum Agenesis | The corpus callosum is the largest white matter structure containing 200 million axons, connecting the two hemispheres of the brain. Agenesis of the c ... Read the Article | 1 | 5 | Activity DO |
| Corpus Callosum Agenesis | The corpus callosum is the largest white matter structure containing 200 million axons, connecting the two hemispheres of the brain. Agenesis of the c ... Read the Article | 1 | 5 | 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 |
| Craniosynostosis | Craniosynostosis results from the premature closure of one or more sutures of the skull. Depending on the number of sutures involved, and the range of ... Read the Article | 1 | 7 | Activity DO |
| Craniosynostosis | Craniosynostosis results from the premature closure of one or more sutures of the skull. Depending on the number of sutures involved, and the range of ... Read the Article | 1 | 7 | Activity MD/PA |
| Crouzon Syndrome | Crouzon syndrome is a genetically inherited syndrome characterized by craniosynostosis (premature fusion of coronal sutures) resulting in the skull an ... Read the Article | 1 | 4 | Activity DO |
| Crouzon Syndrome | Crouzon syndrome is a genetically inherited syndrome characterized by craniosynostosis (premature fusion of coronal sutures) resulting in the skull an ... Read the Article | 1 | 4 | 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 |
| Danon Disease | Danon disease is a rare X-linked dominant genetic disorder that manifests with the clinical triad of cardiomyopathy, skeletal myopathy, and intellectu ... Read the Article | 1 | 6 | Activity DO |
| Danon Disease | Danon disease is a rare X-linked dominant genetic disorder that manifests with the clinical triad of cardiomyopathy, skeletal myopathy, and intellectu ... Read the Article | 1 | 6 | Activity MD/PA |
| Delayed Puberty | Delayed puberty not infrequently occurs in the pediatric population and a common reason for referral to a pediatric endocrinologist. While it is usual ... Read the Article | 1 | 4 | Activity DO |
| Delayed Puberty | Delayed puberty not infrequently occurs in the pediatric population and a common reason for referral to a pediatric endocrinologist. While it is usual ... Read the Article | 1 | 4 | Activity MD/PA |
| Dentatorubral Pallidoluysian Atrophy | Dentatorubral-pallidoluysian atrophy (DRPLA) is a progressive, autosomal dominant disorder with symptoms and severity that vary with the age of onset. ... Read the Article | 1 | 5 | Activity DO |
| Dentatorubral Pallidoluysian Atrophy | Dentatorubral-pallidoluysian atrophy (DRPLA) is a progressive, autosomal dominant disorder with symptoms and severity that vary with the age of onset. ... Read the Article | 1 | 5 | Activity MD/PA |
| Development Milestones | Developmental milestones are markers of a child’s development from infancy on into childhood. They are used to help determine if a child is undergoing ... Read the Article | 1.25 | 9 | Activity DO |
| Development Milestones | Developmental milestones are markers of a child’s development from infancy on into childhood. They are used to help determine if a child is undergoing ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Developmental Delay | Delay in development occurs when the child fails to attain developmental milestones as compared to peers from the same population. It is caused by imp ... Read the Article | 1.25 | 11 | Activity DO |
| Developmental Delay | Delay in development occurs when the child fails to attain developmental milestones as compared to peers from the same population. It is caused by imp ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Developmental Stages of Social Emotional Development In Children | To apply knowledge regarding human growth and development, healthcare professionals need to be aware of 2 areas: (1) milestone competencies, for examp ... Read the Article | 1.75 | 21 | Activity DO |
| Developmental Stages of Social Emotional Development In Children | To apply knowledge regarding human growth and development, healthcare professionals need to be aware of 2 areas: (1) milestone competencies, for examp ... Read the Article | 1.75 | 21 | 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 |
| Disability Evaluation | Impairment and disability are a concern for people around the globe. Injury, illness, or disease that inhibits an individual from participating in the ... Read the Article | 1.25 | 9 | Activity DO |
| Disability Evaluation | Impairment and disability are a concern for people around the globe. Injury, illness, or disease that inhibits an individual from participating in the ... Read the Article | 1.25 | 9 | 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 | 16 | Activity DO |
| Down Syndrome | Down syndrome (trisomy 21) is a genetic disorder caused by the presence of all or a portion of a third chromosome 21. Patients typically present with ... Read the Article | 1.5 | 16 | Activity MD/PA |
| 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 |
| Duplication Cyst | Duplication cysts are rare congenital anomalies of the alimentary tract. The majority of duplication cysts are symptomatic within the first 2 years of ... Read the Article | 1 | 5 | Activity DO |
| Duplication Cyst | Duplication cysts are rare congenital anomalies of the alimentary tract. The majority of duplication cysts are symptomatic within the first 2 years of ... Read the Article | 1 | 5 | Activity MD/PA |
| Dyslexia | Reading is a skill unique to humans and is crucial for living in the world today. Learning to read is one of the first teaching points of elementary s ... Read the Article | 1 | 7 | Activity DO |
| Dyslexia | Reading is a skill unique to humans and is crucial for living in the world today. Learning to read is one of the first teaching points of elementary s ... Read the Article | 1 | 7 | Activity MD/PA |
| Dystonia | Dystonia is defined by involuntary maintained contraction of agonist and antagonist muscles yielding abnormal posturing, twisting and repetitive movem ... Read the Article | 1 | 6 | Activity DO |
| Dystonia | Dystonia is defined by involuntary maintained contraction of agonist and antagonist muscles yielding abnormal posturing, twisting and repetitive movem ... Read the Article | 1 | 6 | 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 |
| Early Childhood Caries | The presence of dental caries in the primary dentition of young children is known as early childhood caries (ECC), which is defined as one or more dec ... Read the Article | 1 | 5 | Activity DO |
| Early Childhood Caries | The presence of dental caries in the primary dentition of young children is known as early childhood caries (ECC), which is defined as one or more dec ... Read the Article | 1 | 5 | Activity MD/PA |
| Echolalia | Echolalia is a meaningless repetition of words or phrases heard by someone. This activity reviews echolalia and highlights different conditions that m ... Read the Article | 1 | 6 | Activity DO |
| Echolalia | Echolalia is a meaningless repetition of words or phrases heard by someone. This activity reviews echolalia and highlights different conditions that m ... Read the Article | 1 | 6 | 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 |
| 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 |
| 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 |
| 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 |
| Enuresis | Enuresis is a common childhood disorder seen in outpatient settings. Enuresis can be promptly treated if cases are identified early. In this activity, ... Read the Article | 1 | 6 | Activity DO |
| Enuresis | Enuresis is a common childhood disorder seen in outpatient settings. Enuresis can be promptly treated if cases are identified early. In this activity, ... Read the Article | 1 | 6 | 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 |
| 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 |
| Feeding Disability In Children | Feeding disability in children is an inadequacy of food intake that results in poor weight gain, failure to thrive, and/or delayed milestones. This ac ... Read the Article | 1 | 6 | Activity DO |
| Feeding Disability In Children | Feeding disability in children is an inadequacy of food intake that results in poor weight gain, failure to thrive, and/or delayed milestones. This ac ... Read the Article | 1 | 6 | Activity MD/PA |
| Fetal Alcohol Syndrome | Fetal alcohol syndrome is one of the five disorders that comprise fetal alcohol spectrum disorders (FASD). These fetal alcohol spectrum disorders clas ... Read the Article | 1 | 6 | Activity DO |
| Fetal Alcohol Syndrome | Fetal alcohol syndrome is one of the five disorders that comprise fetal alcohol spectrum disorders (FASD). These fetal alcohol spectrum disorders clas ... Read the Article | 1 | 6 | Activity MD/PA |
| Fibrodysplasia Ossificans Progressiva | Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes significant disability and morbidity. In this disorder, heterotopic ossif ... Read the Article | 1 | 5 | Activity DO |
| Fibrodysplasia Ossificans Progressiva | Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes significant disability and morbidity. In this disorder, heterotopic ossif ... Read the Article | 1 | 5 | Activity MD/PA |
| Fine Motor Disability | Fine motor disability is an inability or impairment of an individual to perform tasks that require a degree of manual dexterity. Fine motor ability is ... Read the Article | 1 | 5 | Activity DO |
| Fine Motor Disability | Fine motor disability is an inability or impairment of an individual to perform tasks that require a degree of manual dexterity. Fine motor ability is ... Read the Article | 1 | 5 | Activity MD/PA |
| Food Allergies | Food allergy is defined as an immune reaction to proteins in the food and can be immunoglobulin (Ig)E-mediated or non-IgE-mediated. IgE-mediated food ... Read the Article | 1.25 | 8 | Activity DO |
| Food Allergies | Food allergy is defined as an immune reaction to proteins in the food and can be immunoglobulin (Ig)E-mediated or non-IgE-mediated. IgE-mediated food ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Fragile X Syndrome | Fragile X syndrome (FXS), also called Martin-Bell syndrome, is a non-Mendelian trinucleotide repeat disorder. FXS is the most prevalent inherited caus ... Read the Article | 1.25 | 9 | Activity DO |
| Fragile X Syndrome | Fragile X syndrome (FXS), also called Martin-Bell syndrome, is a non-Mendelian trinucleotide repeat disorder. FXS is the most prevalent inherited caus ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Gaucher Disease | Gaucher disease is an autosomal recessive inborn error of metabolism due to the toxic accumulation of glucocerebroside lipids in various organs. It re ... Read the Article | 1.5 | 14 | Activity DO |
| Gaucher Disease | Gaucher disease is an autosomal recessive inborn error of metabolism due to the toxic accumulation of glucocerebroside lipids in various organs. It re ... Read the Article | 1.5 | 14 | Activity MD/PA |
| Genetics and Obesity | Obesity is closely linked to genetics and environmental factors. The newest studies in the field of epigenetics further our understanding of the effec ... Read the Article | 1.25 | 7 | Activity DO |
| Genetics and Obesity | Obesity is closely linked to genetics and environmental factors. The newest studies in the field of epigenetics further our understanding of the effec ... Read the Article | 1.25 | 7 | Activity MD/PA |
| Gerstmann Syndrome | Gerstmann syndrome is a rare neurological disorder consisting of a tetrad of symptoms which include impairment in performing calculations (acalculia), ... Read the Article | 1 | 5 | Activity DO |
| Gerstmann Syndrome | Gerstmann syndrome is a rare neurological disorder consisting of a tetrad of symptoms which include impairment in performing calculations (acalculia), ... Read the Article | 1 | 5 | Activity MD/PA |
| Gout | Gout is one of the most common causes of chronic inflammatory arthritis in the United States, which is characterized by monosodium urate (MSU) monohyd ... Read the Article | 1.5 | 15 | Activity DO |
| Gout | Gout is one of the most common causes of chronic inflammatory arthritis in the United States, which is characterized by monosodium urate (MSU) monohyd ... Read the Article | 1.5 | 15 | 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 |
| Hartnup Disease | Hartnup disease is an autosomal recessive disorder resulting in impaired functioning of transport protein in intestines and kidneys. This results in w ... Read the Article | 1.25 | 9 | Activity DO |
| Hartnup Disease | Hartnup disease is an autosomal recessive disorder resulting in impaired functioning of transport protein in intestines and kidneys. This results in w ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Holoprosencephaly | Holoprosencephaly occurs as a result of anomalous signaling interactions between the neural crest and neural ectoderm. This primarily results in the a ... Read the Article | 1 | 6 | Activity DO |
| Holoprosencephaly | Holoprosencephaly occurs as a result of anomalous signaling interactions between the neural crest and neural ectoderm. This primarily results in the a ... Read the Article | 1 | 6 | Activity MD/PA |
| Human Behavior In A Social Environment | Human behavior in a social environment (HBSE) is a concept that describes a comprehensive view of people and is fundamental to the study of social sci ... Read the Article | 1 | 5 | Activity DO |
| Human Behavior In A Social Environment | Human behavior in a social environment (HBSE) is a concept that describes a comprehensive view of people and is fundamental to the study of social sci ... Read the Article | 1 | 5 | Activity MD/PA |
| Human Growth and Development | Evaluation of growth and development is a crucial element in the physical examination of a patient. A piece of good working knowledge and the skill to ... Read the Article | 1 | 6 | Activity DO |
| Human Growth and Development | Evaluation of growth and development is a crucial element in the physical examination of a patient. A piece of good working knowledge and the skill to ... Read the Article | 1 | 6 | Activity MD/PA |
| Hurler Syndrome | Hurler syndrome, also known as mucopolysaccharidosis type I (MPH I), is one of the eleven mucopolysaccharidoses (MPS) disorders. Hurler syndrome was f ... Read the Article | 1 | 4 | Activity DO |
| Hurler Syndrome | Hurler syndrome, also known as mucopolysaccharidosis type I (MPH I), is one of the eleven mucopolysaccharidoses (MPS) disorders. Hurler syndrome was f ... Read the Article | 1 | 4 | Activity MD/PA |
| Hypomelanosis of Ito | Hypomelanosis of Ito (HI), or pigmentary mosaicism, was previously named incontinentia pigmenti achromians. The disease is currently named hypomelanos ... Read the Article | 1 | 4 | Activity DO |
| Hypomelanosis of Ito | Hypomelanosis of Ito (HI), or pigmentary mosaicism, was previously named incontinentia pigmenti achromians. The disease is currently named hypomelanos ... Read the Article | 1 | 4 | Activity MD/PA |
| Infant Head Lag | Infant head lag is observed when the head seems to flop around or lags posteriorly behind the trunk. Several articles have maintained that head lag sh ... Read the Article | 1 | 5 | Activity DO |
| Infant Head Lag | Infant head lag is observed when the head seems to flop around or lags posteriorly behind the trunk. Several articles have maintained that head lag sh ... Read the Article | 1 | 5 | Activity MD/PA |
| Infantile and Juvenile Scoliosis | Early-onset scoliosis (EOS) occurs in young children and presents a unique and challenging dilemma since the spine, thorax, and lungs are still develo ... Read the Article | 1 | 5 | Activity DO |
| Infantile and Juvenile Scoliosis | Early-onset scoliosis (EOS) occurs in young children and presents a unique and challenging dilemma since the spine, thorax, and lungs are still develo ... Read the Article | 1 | 5 | Activity MD/PA |
| Infantile Cortical Hyperostosis | Infantile cortical hyperostosis (ICH), also known as Caffey disease, was first reported by Roske in 1930 and described by Caffey and Silverman in 1945 ... Read the Article | 1 | 8 | Activity DO |
| Infantile Cortical Hyperostosis | Infantile cortical hyperostosis (ICH), also known as Caffey disease, was first reported by Roske in 1930 and described by Caffey and Silverman in 1945 ... Read the Article | 1 | 8 | Activity MD/PA |
| Infantile Spasm | Infantile spasms are spasms that occur in infancy or early childhood. They are classically characterized by symmetric, brief jerking spells that invol ... Read the Article | 1 | 5 | Activity DO |
| Infantile Spasm | Infantile spasms are spasms that occur in infancy or early childhood. They are classically characterized by symmetric, brief jerking spells that invol ... Read the Article | 1 | 5 | Activity MD/PA |
| Intellectual Disability | Individuals with an intellectual disability have neurodevelopmental deficits characterized by limitations in intellectual functioning and adaptive beh ... Read the Article | 1.75 | 22 | Activity DO |
| Intellectual Disability | Individuals with an intellectual disability have neurodevelopmental deficits characterized by limitations in intellectual functioning and adaptive beh ... Read the Article | 1.75 | 22 | Activity MD/PA |
| Intoeing | Deformities and angular variations of the lower extremities are one of the most common reasons for referral to pediatric orthopedics, with in-toeing s ... Read the Article | 1 | 6 | Activity DO |
| Intoeing | Deformities and angular variations of the lower extremities are one of the most common reasons for referral to pediatric orthopedics, with in-toeing s ... Read the Article | 1 | 6 | Activity MD/PA |
| Jacobs Syndrome | Jacobs syndrome is a rare genetic abnormality in which a male receives an extra Y chromosome from his father. While many patients go undiagnosed due t ... Read the Article | 1 | 7 | Activity DO |
| Jacobs Syndrome | Jacobs syndrome is a rare genetic abnormality in which a male receives an extra Y chromosome from his father. While many patients go undiagnosed due t ... Read the Article | 1 | 7 | Activity MD/PA |
| Juvenile Absence Epilepsy | Juvenile absence epilepsy is an idiopathic generalized epilepsy syndrome that is recognized by the ILAE (International League Against Epilepsy) that t ... Read the Article | 1 | 7 | Activity DO |
| Juvenile Absence Epilepsy | Juvenile absence epilepsy is an idiopathic generalized epilepsy syndrome that is recognized by the ILAE (International League Against Epilepsy) that t ... 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 | 7 | 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 | 7 | Activity MD/PA |
| Kearns Sayre Syndrome | Kearns-Sayre syndrome (KSS) is a subtype of chronic progressive external ophthalmoplegia (CPEO). KSS is defined by the following triad: Onset before t ... Read the Article | 1 | 5 | Activity DO |
| Kearns Sayre Syndrome | Kearns-Sayre syndrome (KSS) is a subtype of chronic progressive external ophthalmoplegia (CPEO). KSS is defined by the following triad: Onset before t ... Read the Article | 1 | 5 | Activity MD/PA |
| Klinefelter Syndrome | Klinefelter syndrome (KS) is the result of 2 or more X chromosomes in a phenotypic male. The clinical phenotype of KS was first described in males wit ... Read the Article | 1.5 | 16 | Activity DO |
| Klinefelter Syndrome | Klinefelter syndrome (KS) is the result of 2 or more X chromosomes in a phenotypic male. The clinical phenotype of KS was first described in males wit ... Read the Article | 1.5 | 16 | 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 |
| Lafora Disease | Lafora disease is a type of progressive myoclonic epilepsy that is inherited in an autosomal recessive manner and typically presents in previously hea ... Read the Article | 1 | 6 | Activity DO |
| Lafora Disease | Lafora disease is a type of progressive myoclonic epilepsy that is inherited in an autosomal recessive manner and typically presents in previously hea ... Read the Article | 1 | 6 | Activity MD/PA |
| Landau Kleffner Syndrome | Landau-Kleffner syndrome is a rare age-related epileptic encephalopathy that usually manifests itself in children aged 3 to 8 years with previously no ... Read the Article | 1 | 5 | Activity DO |
| Landau Kleffner Syndrome | Landau-Kleffner syndrome is a rare age-related epileptic encephalopathy that usually manifests itself in children aged 3 to 8 years with previously no ... Read the Article | 1 | 5 | Activity MD/PA |
| Lead Toxicity | Lead became a common occupational toxin with the birth of the Industrial Revolution, by the end of the 19-century childhood lead poisoning secondary t ... Read the Article | 1.5 | 18 | Activity DO |
| Lead Toxicity | Lead became a common occupational toxin with the birth of the Industrial Revolution, by the end of the 19-century childhood lead poisoning secondary t ... Read the Article | 1.5 | 18 | Activity MD/PA |
| Learning Disability | Learning disabilities (LDs) refer to a number of disorders that may affect the acquisition, organization, retention, comprehension, or the use of both ... Read the Article | 1.25 | 10 | Activity DO |
| Learning Disability | Learning disabilities (LDs) refer to a number of disorders that may affect the acquisition, organization, retention, comprehension, or the use of both ... Read the Article | 1.25 | 10 | Activity MD/PA |
| Legg Calve Perthes Disease | Legg-Calve-Perthes disease (LCPD) is idiopathic osteonecrosis or idiopathic avascular necrosis of the capital femoral epiphysis of the femoral head. T ... Read the Article | 1.25 | 13 | Activity DO |
| Legg Calve Perthes Disease | Legg-Calve-Perthes disease (LCPD) is idiopathic osteonecrosis or idiopathic avascular necrosis of the capital femoral epiphysis of the femoral head. T ... Read the Article | 1.25 | 13 | Activity MD/PA |
| Lennox Gastaut Syndrome | Lennox-Gastaut syndrome (LGS) is a rare but severe form of childhood epilepsy. LGS is characterized by a triad of multiple seizure types, characterist ... Read the Article | 1 | 5 | Activity DO |
| Lennox Gastaut Syndrome | Lennox-Gastaut syndrome (LGS) is a rare but severe form of childhood epilepsy. LGS is characterized by a triad of multiple seizure types, characterist ... Read the Article | 1 | 5 | Activity MD/PA |
| Lesch Nyhan Syndrome | Lesch Nyhan Syndrome is an inborn disorder caused by a deficiency of hypoxanthine-guanine phosphoribosyltransferase (HPRT) enzyme, an enzyme of purine ... Read the Article | 1.25 | 11 | Activity DO |
| Lesch Nyhan Syndrome | Lesch Nyhan Syndrome is an inborn disorder caused by a deficiency of hypoxanthine-guanine phosphoribosyltransferase (HPRT) enzyme, an enzyme of purine ... Read the Article | 1.25 | 11 | Activity MD/PA |
| Lichen Nitidus | Lichen nitidus is a rare benign condition characterized by extensive 1- to 2-mm skin-colored papules commonly occurring on upper extremities, chest, a ... Read the Article | 1 | 6 | Activity DO |
| Lichen Nitidus | Lichen nitidus is a rare benign condition characterized by extensive 1- to 2-mm skin-colored papules commonly occurring on upper extremities, chest, a ... 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 |
| Lysosomal Storage Disease | Lysosomal storage diseases (LSDs) are inborn errors of metabolism characterized by the accumulation of substrates in excess in various organs' cells d ... Read the Article | 1 | 5 | Activity DO |
| Lysosomal Storage Disease | Lysosomal storage diseases (LSDs) are inborn errors of metabolism characterized by the accumulation of substrates in excess in various organs' cells d ... Read the Article | 1 | 5 | Activity MD/PA |
| Macrocephaly | Macrocephaly is the condition in which the head circumference of an infant is above 2 standard deviations, which is above the 97th percentile. It can ... Read the Article | 1 | 5 | Activity DO |
| Macrocephaly | Macrocephaly is the condition in which the head circumference of an infant is above 2 standard deviations, which is above the 97th percentile. It can ... 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 |
| 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 |
| Marijuana And Maternal, Perinatal, and Neonatal Outcomes | Drug use and drug dependency are major public health problems. Marijuana is one of the most commonly used drugs among all genders and age groups. This ... Read the Article | 1 | 5 | Activity DO |
| Marijuana And Maternal, Perinatal, and Neonatal Outcomes | Drug use and drug dependency are major public health problems. Marijuana is one of the most commonly used drugs among all genders and age groups. This ... Read the Article | 1 | 5 | Activity MD/PA |
| 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 |
| Melas Syndrome | Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) is a mitochondrial disease primarily affecting the nervous system an ... Read the Article | 1 | 6 | Activity DO |
| Melas Syndrome | Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) is a mitochondrial disease primarily affecting the nervous system an ... Read the Article | 1 | 6 | 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 |
| 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 |
| 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 Neoplasia Type 1 | Multiple endocrine neoplasia Type 1 (MEN1), also known as Wermer syndrome, is a rare hereditary endocrine tumor syndrome. The most common tumors seen ... Read the Article | 1.25 | 7 | Activity DO |
| Multiple Endocrine Neoplasia Type 1 | Multiple endocrine neoplasia Type 1 (MEN1), also known as Wermer syndrome, is a rare hereditary endocrine tumor syndrome. The most common tumors seen ... Read the Article | 1.25 | 7 | 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 |
| Myoclonic Epilepsy Of Infancy | Myoclonic epilepsy of infancy is a rare self-limited epileptic syndrome characterized by brief myoclonic seizures in previously healthy and developmen ... Read the Article | 1 | 5 | Activity DO |
| Myoclonic Epilepsy Of Infancy | Myoclonic epilepsy of infancy is a rare self-limited epileptic syndrome characterized by brief myoclonic seizures in previously healthy and developmen ... Read the Article | 1 | 5 | Activity MD/PA |
| Myotonia Congenita | Myotonia congenita (MC) is a genetic neuromuscular channelopathy which usually presents in early childhood resulting in a delay of skeletal muscle rel ... Read the Article | 1 | 6 | Activity DO |
| Myotonia Congenita | Myotonia congenita (MC) is a genetic neuromuscular channelopathy which usually presents in early childhood resulting in a delay of skeletal muscle rel ... Read the Article | 1 | 6 | 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 |
| Neural Tube Disorders | Neural tube defects are the most common severe central nervous system anomalies, only second to cardiovascular abnormalities resulting in congenital m ... Read the Article | 1.5 | 13 | Activity DO |
| Neural Tube Disorders | Neural tube defects are the most common severe central nervous system anomalies, only second to cardiovascular abnormalities resulting in congenital m ... Read the Article | 1.5 | 13 | Activity MD/PA |
| Neurocutaneous Syndromes | As the name implies, neurocutaneous syndromes are disorders involving the nervous system and the skin. Two of the most common neurocutaneous syndrome ... Read the Article | 1 | 4 | Activity DO |
| Neurocutaneous Syndromes | As the name implies, neurocutaneous syndromes are disorders involving the nervous system and the skin. Two of the most common neurocutaneous syndrome ... Read the Article | 1 | 4 | Activity MD/PA |
| Neurofibroma | Neurofibromas are the most common peripheral nerve sheath tumor and are often found either by patients or during routine skin exams. These lesions app ... Read the Article | 1.25 | 9 | Activity DO |
| Neurofibroma | Neurofibromas are the most common peripheral nerve sheath tumor and are often found either by patients or during routine skin exams. These lesions app ... Read the Article | 1.25 | 9 | 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 |
| Niemann-Pick Disease | The management of Niemann-Pick disease and new approaches have been recently introduced. To achieve optimal outcomes, the basic and clinical aspects ... Read the Article | 1.25 | 8 | Activity DO |
| Niemann-Pick Disease | The management of Niemann-Pick disease and new approaches have been recently introduced. To achieve optimal outcomes, the basic and clinical aspects ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Nocturnal Enuresis | Enuresis refers to the involuntary loss of urine during sleep that occurs at least twice a week in children older than 5 years of age (or the developm ... Read the Article | 1 | 6 | Activity DO |
| Nocturnal Enuresis | Enuresis refers to the involuntary loss of urine during sleep that occurs at least twice a week in children older than 5 years of age (or the developm ... Read the Article | 1 | 6 | 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 in Pediatric Patients | Obesity is a common health concern in pediatrics. It causes a myriad of comorbidities affecting every organ system of the child. Inadequate treatment ... Read the Article | 1 | 5 | Activity DO |
| Obesity in Pediatric Patients | Obesity is a common health concern in pediatrics. It causes a myriad of comorbidities affecting every organ system of the child. Inadequate treatment ... Read the Article | 1 | 5 | Activity MD/PA |
| Opisthotonus | Opisthotonus is defined as a dramatic abnormal posture due to spastic contraction of the extensor muscles of the neck, trunk, and lower extremities th ... Read the Article | 1 | 4 | Activity DO |
| Opisthotonus | Opisthotonus is defined as a dramatic abnormal posture due to spastic contraction of the extensor muscles of the neck, trunk, and lower extremities th ... Read the Article | 1 | 4 | Activity MD/PA |
| Oppositional Defiant Disorder | Oppositional defiant disorder (ODD) is a type of childhood disruptive behavior disorder that primarily involves problems with the self-control of emot ... Read the Article | 1 | 6 | Activity DO |
| Oppositional Defiant Disorder | Oppositional defiant disorder (ODD) is a type of childhood disruptive behavior disorder that primarily involves problems with the self-control of emot ... Read the Article | 1 | 6 | Activity MD/PA |
| Opsoclonus | Opsoclonus is an oculomotor dyskinesia characterized by rapid, repetitive conjugate eye movements that are involuntary, arrhythmic, chaotic, and multi ... Read the Article | 1 | 5 | Activity DO |
| Opsoclonus | Opsoclonus is an oculomotor dyskinesia characterized by rapid, repetitive conjugate eye movements that are involuntary, arrhythmic, chaotic, and multi ... Read the Article | 1 | 5 | Activity MD/PA |
| Osteopetrosis | The name osteopetrosis encompasses a group of hereditary metabolic bone diseases, all of which detrimentally affect bone growth and remodeling leading ... Read the Article | 1 | 6 | Activity DO |
| Osteopetrosis | The name osteopetrosis encompasses a group of hereditary metabolic bone diseases, all of which detrimentally affect bone growth and remodeling leading ... Read the Article | 1 | 6 | Activity MD/PA |
| Parry Romberg Syndrome | Parry Romberg syndrome (PRS) or progressive hemifacial atrophy is a progressive idiopathic disorder, presenting in early childhood, with a spontaneous ... Read the Article | 1 | 5 | Activity DO |
| Parry Romberg Syndrome | Parry Romberg syndrome (PRS) or progressive hemifacial atrophy is a progressive idiopathic disorder, presenting in early childhood, with a spontaneous ... Read the Article | 1 | 5 | Activity MD/PA |
| Pediatric Abusive Head Trauma | Pediatric abusive head trauma (AHT), or shaken baby syndrome, most often involves shaking, blunt impact, or a combination of both in infants and young ... Read the Article | 2 | 24 | Activity DO |
| Pediatric Abusive Head Trauma | Pediatric abusive head trauma (AHT), or shaken baby syndrome, most often involves shaking, blunt impact, or a combination of both in infants and young ... Read the Article | 2 | 24 | Activity MD/PA |
| Pediatric Hearing Loss | Pediatric hearing loss is a broad category that covers a wide range of pathologies. Early detection and prompt management are essential, as the develo ... Read the Article | 1 | 5 | Activity DO |
| Pediatric Hearing Loss | Pediatric hearing loss is a broad category that covers a wide range of pathologies. Early detection and prompt management are essential, as the develo ... Read the Article | 1 | 5 | Activity MD/PA |
| Pediatric Umbilical Hernia | An umbilical hernia presents as a bulge at the site of the umbilicus; it is a common finding during routine well-baby visits for the first few months ... Read the Article | 1 | 7 | Activity DO |
| Pediatric Umbilical Hernia | An umbilical hernia presents as a bulge at the site of the umbilicus; it is a common finding during routine well-baby visits for the first few months ... Read the Article | 1 | 7 | Activity MD/PA |
| 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 |
| Pes Cavus | Pes cavus is an orthopedic condition that manifests in both children and adults. It is defined primarily by the elevation of the longitudinal arch of ... Read the Article | 1.25 | 9 | Activity DO |
| Pes Cavus | Pes cavus is an orthopedic condition that manifests in both children and adults. It is defined primarily by the elevation of the longitudinal arch of ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Pfeiffer Syndrome | Pfeiffer syndrome is an inherited craniofacial disorder that is associated with primary craniosynostosis, midface hypoplasia, broad thumbs and great t ... Read the Article | 1 | 6 | Activity DO |
| Pfeiffer Syndrome | Pfeiffer syndrome is an inherited craniofacial disorder that is associated with primary craniosynostosis, midface hypoplasia, broad thumbs and great t ... Read the Article | 1 | 6 | Activity MD/PA |
| PHACE Syndrome | Infantile hemangioma is the most prevalent benign tumor of infancy, with an estimated incidence between 4 and 5 percent. Large facial segmental hemang ... Read the Article | 1 | 7 | Activity DO |
| PHACE Syndrome | Infantile hemangioma is the most prevalent benign tumor of infancy, with an estimated incidence between 4 and 5 percent. Large facial segmental hemang ... Read the Article | 1 | 7 | Activity MD/PA |
| Phenylketonuria | Phenylketonuria (PKU) is an inborn error of metabolism (IEM) most often caused by missense mutations in the gene encoding phenylalanine hydroxylase (P ... Read the Article | 1.25 | 13 | Activity DO |
| Phenylketonuria | Phenylketonuria (PKU) is an inborn error of metabolism (IEM) most often caused by missense mutations in the gene encoding phenylalanine hydroxylase (P ... Read the Article | 1.25 | 13 | Activity MD/PA |
| Pica | The American Psychiatric Association's Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) defines pica as eating non-nutriti ... Read the Article | 1 | 4 | Activity DO |
| Pica | The American Psychiatric Association's Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) defines pica as eating non-nutriti ... Read the Article | 1 | 4 | 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 |
| Plagiocephaly | Plagiocephaly is defined as an asymmetric shape of the head due to unilateral flattening. The term flathead can be used as a synonym. Plagiocephaly ca ... Read the Article | 1 | 6 | Activity DO |
| Plagiocephaly | Plagiocephaly is defined as an asymmetric shape of the head due to unilateral flattening. The term flathead can be used as a synonym. Plagiocephaly ca ... Read the Article | 1 | 6 | Activity MD/PA |
| 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 |
| Poikiloderma Congenitale | Congenital poikiloderma, also known as Rothmund-Thomson syndrome (RTS), is a rare genodermatosis with autosomal recessive inheritance. It is character ... Read the Article | 1 | 4 | Activity DO |
| Poikiloderma Congenitale | Congenital poikiloderma, also known as Rothmund-Thomson syndrome (RTS), is a rare genodermatosis with autosomal recessive inheritance. It is character ... Read the Article | 1 | 4 | Activity MD/PA |
| 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 |
| Rapid Eye Movement Sleep Behavior Disorder | Rapid eye movement behavior disorder (RBD) is a type of parasomnia that has a strong link to neurodegenerative diseases. It can also be very disturbin ... Read the Article | 1 | 5 | Activity DO |
| Rapid Eye Movement Sleep Behavior Disorder | Rapid eye movement behavior disorder (RBD) is a type of parasomnia that has a strong link to neurodegenerative diseases. It can also be very disturbin ... Read the Article | 1 | 5 | Activity MD/PA |
| Rett Syndrome | Rett syndrome (RTT) is a neurodevelopmental disorder that should be considered in a child who demonstrates regression in previously acquired skills af ... Read the Article | 1.25 | 8 | Activity DO |
| Rett Syndrome | Rett syndrome (RTT) is a neurodevelopmental disorder that should be considered in a child who demonstrates regression in previously acquired skills af ... Read the Article | 1.25 | 8 | Activity MD/PA |
| Rolandic Epilepsy Seizure | Benign rolandic epilepsy (BRE), also called benign epilepsy with centrotemporal spikes (BECTS) or benign epilepsy of childhood with centrotemporal spi ... Read the Article | 1 | 6 | Activity DO |
| Rolandic Epilepsy Seizure | Benign rolandic epilepsy (BRE), also called benign epilepsy with centrotemporal spikes (BECTS) or benign epilepsy of childhood with centrotemporal spi ... Read the Article | 1 | 6 | 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 | 1.25 | 9 | 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 | 1.25 | 9 | Activity MD/PA |
| Sensory and Perceptual Alterations | Sensory-perceptual alteration can be defined as when there is a change in the pattern of sensory stimuli, followed by an abnormal response to such sti ... Read the Article | 1 | 4 | Activity DO |
| Sensory and Perceptual Alterations | Sensory-perceptual alteration can be defined as when there is a change in the pattern of sensory stimuli, followed by an abnormal response to such sti ... Read the Article | 1 | 4 | Activity MD/PA |
| Slipped Capital Femoral Epiphysis | Slipped capital femoral epiphysis (slipped upper femoral epiphysis), is a common hip pathology in pre-adolescents and adolescents. It occurs when the ... Read the Article | 1.5 | 17 | Activity DO |
| Slipped Capital Femoral Epiphysis | Slipped capital femoral epiphysis (slipped upper femoral epiphysis), is a common hip pathology in pre-adolescents and adolescents. It occurs when the ... Read the Article | 1.5 | 17 | 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 |
| Spasticity | Spasticity, which is sometimes referred to as tightness or stiffness, is a motor disorder marked by a velocity-dependent increase in muscle tone or to ... Read the Article | 1 | 6 | Activity DO |
| Spasticity | Spasticity, which is sometimes referred to as tightness or stiffness, is a motor disorder marked by a velocity-dependent increase in muscle tone or to ... Read the Article | 1 | 6 | Activity MD/PA |
| Spinal Muscle Atrophy | Spinal muscular atrophy is an inherited autosomal recessive disease of a varying phenotype that is characterized by progressive muscle weakness, reduc ... Read the Article | 1.25 | 7 | Activity DO |
| Spinal Muscle Atrophy | Spinal muscular atrophy is an inherited autosomal recessive disease of a varying phenotype that is characterized by progressive muscle weakness, reduc ... Read the Article | 1.25 | 7 | Activity MD/PA |
| 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 |
| 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 | 12 | 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 | 12 | 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 |
| Supernumerary Digit | Polydactyly or supernumerary digit is a common malformation. It involves mostly the upper limbs. Classifications have been established to ease its man ... Read the Article | 1 | 5 | Activity DO |
| Supernumerary Digit | Polydactyly or supernumerary digit is a common malformation. It involves mostly the upper limbs. Classifications have been established to ease its man ... Read the Article | 1 | 5 | Activity MD/PA |
| Supravalvar Aortic Stenosis | Supravalvular aortic stenosis (SVAS) is a congenital heart defect that accounts for 8 to 14 percent of all cases of congenital aortic stenosis. It inv ... Read the Article | 1 | 4 | Activity DO |
| Supravalvar Aortic Stenosis | Supravalvular aortic stenosis (SVAS) is a congenital heart defect that accounts for 8 to 14 percent of all cases of congenital aortic stenosis. It inv ... Read the Article | 1 | 4 | Activity MD/PA |
| 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 |
| Syndromic Sensorineural Hearing Loss | Congenital hearing loss affects 1 to 3 per 1000 newborns. For many children born with hearing loss, it is an isolated finding known as a non-syndromic ... Read the Article | 1 | 5 | Activity DO |
| Syndromic Sensorineural Hearing Loss | Congenital hearing loss affects 1 to 3 per 1000 newborns. For many children born with hearing loss, it is an isolated finding known as a non-syndromic ... Read the Article | 1 | 5 | Activity MD/PA |
| Tangier Disease | Tangier disease occurs due to the accumulation of cholesterol esters within a body organ. This activity outlines the evaluation and management of it a ... Read the Article | 1 | 5 | Activity DO |
| Tangier Disease | Tangier disease occurs due to the accumulation of cholesterol esters within a body organ. This activity outlines the evaluation and management of it a ... Read the Article | 1 | 5 | Activity MD/PA |
| Tay-Sachs Disease | Tay Sachs disease is a rare autosomal recessive progressive neurodegenerative disorder. Patients usually exhibit a severe clinical course with death i ... Read the Article | 1.75 | 22 | Activity DO |
| Tay-Sachs Disease | Tay Sachs disease is a rare autosomal recessive progressive neurodegenerative disorder. Patients usually exhibit a severe clinical course with death i ... Read the Article | 1.75 | 22 | Activity MD/PA |
| Temper Tantrums | Although temper tantrums are a normal part of development in toddlers, they can be distressing for caregivers and families. This activity describes ch ... Read the Article | 1 | 3 | Activity DO |
| Temper Tantrums | Although temper tantrums are a normal part of development in toddlers, they can be distressing for caregivers and families. This activity describes ch ... Read the Article | 1 | 3 | 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 |
| Thumb Sucking | Thumb sucking is a behavior that can be grouped under a list of habits known as non–nutritive sucking habits. Within this group, we can also find the ... Read the Article | 1 | 3 | Activity DO |
| Thumb Sucking | Thumb sucking is a behavior that can be grouped under a list of habits known as non–nutritive sucking habits. Within this group, we can also find the ... Read the Article | 1 | 3 | Activity MD/PA |
| Tourette Syndrome And Other Tic Disorders | Tourette syndrome, also referred to as Tourette disorder, is a common neurodevelopmental disorder affecting up to 1 percent of the population. It is c ... Read the Article | 1.75 | 20 | Activity DO |
| Tourette Syndrome And Other Tic Disorders | Tourette syndrome, also referred to as Tourette disorder, is a common neurodevelopmental disorder affecting up to 1 percent of the population. It is c ... Read the Article | 1.75 | 20 | Activity MD/PA |
| Tracheoesophageal Fistula | Tracheoesophageal fistulas (TEFs) represent one of the most common congenital anomalies seen in major pediatric surgical centers. Infants with tracheo ... Read the Article | 1.25 | 8 | Activity DO |
| Tracheoesophageal Fistula | Tracheoesophageal fistulas (TEFs) represent one of the most common congenital anomalies seen in major pediatric surgical centers. Infants with tracheo ... Read the Article | 1.25 | 8 | Activity MD/PA |
| 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 |
| Truncus Arteriosus | Persistent truncus arteriosus (TA) is a rare, congenital, cyanotic heart defect characterized by a ventricular septal defect (VSD), a single truncal v ... Read the Article | 1.25 | 9 | Activity DO |
| Truncus Arteriosus | Persistent truncus arteriosus (TA) is a rare, congenital, cyanotic heart defect characterized by a ventricular septal defect (VSD), a single truncal v ... Read the Article | 1.25 | 9 | Activity MD/PA |
| Tuberous Sclerosis | Tuberous sclerosis complex (TSC) is a genetic disorder that affects multiple systems. It is inherited in an autosomal dominant fashion and is characte ... Read the Article | 2.25 | 32 | Activity DO |
| Tuberous Sclerosis | Tuberous sclerosis complex (TSC) is a genetic disorder that affects multiple systems. It is inherited in an autosomal dominant fashion and is characte ... Read the Article | 2.25 | 32 | Activity MD/PA |
| Turner Syndrome | Turner syndrome, also referred to as congenital ovarian hypoplasia syndrome is the most common sex chromosomal abnormality found in females. It result ... Read the Article | 1.5 | 19 | Activity DO |
| Turner Syndrome | Turner syndrome, also referred to as congenital ovarian hypoplasia syndrome is the most common sex chromosomal abnormality found in females. It result ... Read the Article | 1.5 | 19 | Activity MD/PA |
| Upper Airway Resistance Syndrome | Upper airway resistance syndrome, commonly known as UARS, is a disorder included with many others that encompass an umbrella of conditions characteriz ... Read the Article | 1 | 6 | Activity DO |
| Upper Airway Resistance Syndrome | Upper airway resistance syndrome, commonly known as UARS, is a disorder included with many others that encompass an umbrella of conditions characteriz ... Read the Article | 1 | 6 | Activity MD/PA |
| Urea Cycle Disorders | Urea cycle disorders are inborn errors of metabolism resulting from defects in one of the enzymes or transporter molecules involved in the hepatic rem ... Read the Article | 1.25 | 8 | Activity DO |
| Urea Cycle Disorders | Urea cycle disorders are inborn errors of metabolism resulting from defects in one of the enzymes or transporter molecules involved in the hepatic rem ... Read the Article | 1.25 | 8 | Activity MD/PA |
| 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 |
| Vigabatrin | Vigabatrin is a medication used in the management and treatment of infantile spasms and refractory complex partial seizures. It is in the anti-epilept ... Read the Article | 1 | 5 | Activity DO |
| Vigabatrin | Vigabatrin is a medication used in the management and treatment of infantile spasms and refractory complex partial seizures. It is in the anti-epilept ... Read the Article | 1 | 5 | Activity MD/PA |
| Vohwinkel Syndrome | Vohwinkel syndrome, also known as keratoderma hereditarian mutilans, is classified as a type of hereditary palmoplantar keratoderma (PPK). Classicall ... Read the Article | 1 | 4 | Activity DO |
| Vohwinkel Syndrome | Vohwinkel syndrome, also known as keratoderma hereditarian mutilans, is classified as a type of hereditary palmoplantar keratoderma (PPK). Classicall ... Read the Article | 1 | 4 | 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 |
| 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 |
| Wyburn-Mason Syndrome | Wyburn-Mason syndrome is a rare nonhereditary congenital phakomatoses which presents with multiple arteriovenous malformations that tend to be large a ... Read the Article | 1 | 7 | Activity DO |
| Wyburn-Mason Syndrome | Wyburn-Mason syndrome is a rare nonhereditary congenital phakomatoses which presents with multiple arteriovenous malformations that tend to be large a ... Read the Article | 1 | 7 | 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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