Pediatric-Developmental CME
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Pediatric-Developmental Articles (180)
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 |
| 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 |
| 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 | 5 | 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 | 5 | 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 |
| 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 |
| 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 |
| 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 | 22 | 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 | 22 | 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 |
| 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 | 6 | 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 | 6 | 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 |
| 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 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 | 8 | 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 | 8 | 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 |
| 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 |
| 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 | 5 | 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 | 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 |
| 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 |
| 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 |
| 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 | 17 | 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 | 17 | 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 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 | 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 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 | 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 |
| 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 | 5 | 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 | 5 | 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 | 17 | 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 | 17 | 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 | 9 | 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 | 9 | 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 | 12 | 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 | 12 | 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 | 12 | 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 | 12 | 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 abuse and drug dependency are major public health problems. Marijuana is the most commonly abused drug among all genders and age groups. This act ... Read the Article | 1 | 5 | Activity DO |
| Marijuana And Maternal, Perinatal, and Neonatal Outcomes | Drug abuse and drug dependency are major public health problems. Marijuana is the most commonly abused drug among all genders and age groups. This act ... 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 | 8 | 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 | 8 | 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 |
| 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 Obstructive Sleep Apnea | Obstructive sleep apnea (OSA) is an essential topic in pediatrics that is frequently overlooked, especially in the context of children with neurodevel ... Read the Article | 1 | 6 | Activity DO |
| Pediatric Obstructive Sleep Apnea | Obstructive sleep apnea (OSA) is an essential topic in pediatrics that is frequently overlooked, especially in the context of children with neurodevel ... Read the Article | 1 | 6 | 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 |
| 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 |
| 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 | 7 | 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 | 7 | 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 | 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 |
| 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 |
| 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 | 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 |
| 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 |
| 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 | 8 | 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 | 8 | 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 | 31 | 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 | 31 | 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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