SettingsNeurological disorders in children
Adrenoleukodystrophy
Adrenoleukodystrophy (ALD, also called Siemerling-Creutzfeldt Disease or Schilder's disease) is a rare, inherited disorder that leads to progressive brain damage, failure of the adre...
Adrenoleukodystrophy (ALD, also called Siemerling-Creutzfeldt Disease or Schilder's disease) is a rare, inherited disorder that leads to progressive brain damage, failure of the adre...
Aicardi syndrome
Aicardi syndrome is a rare genetic malformation syndrome characterized by the partial or complete absence of a key structure in the brain called the corpus callosum, the presence of retinal abno...
Aicardi syndrome is a rare genetic malformation syndrome characterized by the partial or complete absence of a key structure in the brain called the corpus callosum, the presence of retinal abno...
Alexander disease
Alexander disease is a slowly progressing and fatal neurodegenerative disease.
Alexander disease is a slowly progressing and fatal neurodegenerative disease.
Amblyaudia
Amblyaudia is a brain based hearing disorder that results from auditory deprivation during critical periods of brain development1.
Amblyaudia is a brain based hearing disorder that results from auditory deprivation during critical periods of brain development1.
Asperger syndrome
Asperger syndrome, also known as Asperger's syndrome or Asperger disorder, is an autism spectrum disorder that is characterized by significant difficulties in social interaction, alo...
Asperger syndrome, also known as Asperger's syndrome or Asperger disorder, is an autism spectrum disorder that is characterized by significant difficulties in social interaction, alo...
Autism
Autism is a disorder of neural development characterized by impaired social interaction and communication, and by restricted and repetitive behavior.
Autism is a disorder of neural development characterized by impaired social interaction and communication, and by restricted and repetitive behavior.
Canavan disease
Canavan disease, also called Canavan-Van Bogaert-Bertrand disease, aspartoacylase deficiency or aminoacylase 2 deficiency, is an autosomal recessive degenerative disorder that ...
Canavan disease, also called Canavan-Van Bogaert-Bertrand disease, aspartoacylase deficiency or aminoacylase 2 deficiency, is an autosomal recessive degenerative disorder that ...
Cerebral palsy
Cerebral palsy is an umbrella term encompassing a group of non-progressive, non-contagious motor conditions that cause physical disability in human development, chiefly in the various areas of b...
Cerebral palsy is an umbrella term encompassing a group of non-progressive, non-contagious motor conditions that cause physical disability in human development, chiefly in the various areas of b...
Childhood disintegrative disorder
Childhood disintegrative disorder (CDD), also known as Heller's syndrome and disintegrative psychosis, is a rare (1.7 cases per 100,000) condition characterized by late onset (...
Childhood disintegrative disorder (CDD), also known as Heller's syndrome and disintegrative psychosis, is a rare (1.7 cases per 100,000) condition characterized by late onset (...
DynaVox
DynaVox Mayer-Johnson is a US-based developer, manufacturer and distributor of Speech Generating Devices headquartered in Pittsburgh, PA. The company was formed in 1983 and has since become the ...
DynaVox Mayer-Johnson is a US-based developer, manufacturer and distributor of Speech Generating Devices headquartered in Pittsburgh, PA. The company was formed in 1983 and has since become the ...
Krabbe disease
Krabbe disease (also known as globoid cell leukodystrophy or galactosylceramide lipidosis) is a rare, often fatal degenerative disorder that affects the myelin sheath of the nervous ...
Krabbe disease (also known as globoid cell leukodystrophy or galactosylceramide lipidosis) is a rare, often fatal degenerative disorder that affects the myelin sheath of the nervous ...
Leigh's disease
Leigh's disease, also known as Subacute Necrotizing Encephalomyelopathy, is a rare neurometabolic disorder that affects the central nervous system.
Leigh's disease, also known as Subacute Necrotizing Encephalomyelopathy, is a rare neurometabolic disorder that affects the central nervous system.
Metachromatic leukodystrophy
Metachromatic leukodystrophy is a lysosomal storage disease which is commonly listed in the family of leukodystrophies.
Metachromatic leukodystrophy is a lysosomal storage disease which is commonly listed in the family of leukodystrophies.
Myoclonic Astatic Epilepsy
Myoclonic astatic epilepsy, also known as Doose syndrome, is a generalized idiopathic epilepsy.
Myoclonic astatic epilepsy, also known as Doose syndrome, is a generalized idiopathic epilepsy.
Myoclonic astatic epilepsy
Myoclonic astatic epilepsy, also known as Doose syndrome, is a generalized idiopathic epilepsy.
Myoclonic astatic epilepsy, also known as Doose syndrome, is a generalized idiopathic epilepsy.
PDD-NOS
Pervasive Developmental Disorder—Not Otherwise Specified is a pervasive developmental disorder, also called an autism spectrum disorder.
Pervasive Developmental Disorder—Not Otherwise Specified is a pervasive developmental disorder, also called an autism spectrum disorder.
Pervasive developmental disorder
Pervasive developmental disorders is a diagnostic category refers to a group of disorders characterized by delays or impairments in communication, social behaviors, and cognitive development.Per...
Pervasive developmental disorders is a diagnostic category refers to a group of disorders characterized by delays or impairments in communication, social behaviors, and cognitive development.Per...
Progressive rubella panencephalitis
Progressive rubella panencephalitis is a neurological disorder which may occur in a child with congenital rubella.
Progressive rubella panencephalitis is a neurological disorder which may occur in a child with congenital rubella.
Rett syndrome
Rett syndrome is a neurodevelopmental disorder jacob is a form of named particular to this syndrome of the grey matter of the brain that almost exclusively affects females.
Rett syndrome is a neurodevelopmental disorder jacob is a form of named particular to this syndrome of the grey matter of the brain that almost exclusively affects females.
Tay-Sachs disease
Tay–Sachs disease (abbreviated TSD, also known as GM2 gangliosidosis or Hexosaminidase A deficiency) is an autosomal recessive genetic disorder.
Tay–Sachs disease (abbreviated TSD, also known as GM2 gangliosidosis or Hexosaminidase A deficiency) is an autosomal recessive genetic disorder.
Tay–Sachs disease
Tay–Sachs disease is an autosomal recessive genetic disorder.
Tay–Sachs disease is an autosomal recessive genetic disorder.