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bn:02779251n

Noun Concept

Categories: Articles requiring reliable medical sources, Intellectual disability, Syndromes affecting the nervous system, Epilepsy types, Citation overkill

early infantile epileptic encephalopathy 9 epilepsy-intellectual disability in females Epilepsy in females with mental retardation Developmental and epileptic encephalopathy 9 early infantile female-limited epilecptic encephalopathy

Epilepsy-intellectual disability in females also known as PCDH19 gene-related epilepsy or epileptic encephalopathy, early infantile, 9, is a rare type of epilepsy that affects predominately females and is characterized by clusters of brief seizures, which start in infancy or early childhood, and is occasionally accompanied by varying degrees of cognitive impairment. Wikipedia

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Infantile epileptic encephalopathy that has material basis in the gene encoding protocadherin-19 (PCDH19) on chromosome Xq22 Wikidata

IS A

rare disease

epilepsy

Ohtahara syndrome

Wikipedia

epilepsy-intellectual disability in females

Wikidata

early infantile epileptic encephalopathy 9

Wikipedia Redirections

Developmental and epileptic encephalopathy 9, EIEE9, Epilepsy and mental retardation restricted to females, Epilepsy female Restricted, Epilepsy in females with intellectual disability, Epilepsy in females with mental retardation, Epilepsy in Females with Mental Retardation, epileptic encephalopathy, early infantile, 9, Juberg-Hellman Syndrome

Wikidata Alias

early infantile female-limited epilecptic encephalopathy, EFMR, EIEE9, Epilepsy and mental retardation limited to females, female restricted epilepsy with mental retardation, Juberg Hellman syndrome, PCDH19-related epilepsy, PCDH19 Epilepsy, PCDH19 female pediatric epilepsy, PCDH19 related syndrome, Protocadherin 19 (PCDH19)-related epilepsy