Rolandic epilepsy-speech dyspraxia syndrome
ORPHA:163721· ICD-10 G40.8
Definition
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.
- Prevalence
- Unknown
- Inheritance
- Autosomal dominant, X-linked dominant
- Age of onset
- Antenatal, Infancy, Neonatal