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