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Синдром роландичної епілепсії та мовленнєвої диспраксії

ORPHA:163721· ICD-10 G40.8· Rolandic epilepsy-speech dyspraxia syndrome

Визначення(English summary)

Rolandic epilepsy-speech dyspraxia syndrome is a rare, genetic epilepsy characterized by speech disorder (including a range of symptoms from dysarthria, speech dyspraxia, receptive and expressive language delay/regression and acquired aphasia to subtle impairments of conversational speech) and epilepsy (mostly focal and secondary generalized childhood-onset seizures, sometimes with aura). Mild to severe intellectual disability may also be observed.

Поширеність
Unknown
Успадкування
Autosomal dominant, X-linked dominant
Вік початку
Antenatal, Infancy, Neonatal