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Developmental and epileptic encephalopathy, 9
rareFemale restricted epilepsy with intellectual disability is a rare X-linked epilepsy syndrome characterized by febrile or afebrile seizures (mainly tonic-clonic, but also absence, myoclonic, and atonic) starting in the first years of life and, in most cases, developmental delay and intellectual disability of variable severity. Behavioral disturbances (e.g. autistic features, hyperactivity, and aggressiveness) are also frequently associated. This disease affects exclusively females, with male carriers being unaffected, despite an X-linked inheritance.
- Identifiers
- MONDO:0010246 OMIM:300088Orphanet:101039
- Causal genes
- PCDH19
- Part of
- X-linked complex neurodevelopmental disorderX-linked intellectual disability-epilepsy syndromeGenetic developmental and epileptic encephalopathy
- Also known as
- DEE9 · developmental and epileptic encephalopathy 9 · early infantile epileptic encephalopathy caused by mutation in PCDH19 · early infantile epileptic encephalopathy type 9 · EFMR
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