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CNTNAP2-залежна епілептична енцефалопатія розвитку

ORPHA:163681· ICD-10 Q04.8· CNTNAP2-related developmental and epileptic encephalopathy

Визначення(English summary)

A rare, genetic, syndromic neurodevelopmental disorder characterized by moderate to mostly severe intellectual disability, speech impairment with normal or mildly delayed motor development and early-onset seizures often accompanied by developmental regression. Autistic behavior and stereotypic movements are common.

Поширеність
Unknown
Успадкування
Autosomal recessive
Вік початку
Infancy