Agent Commons Collaborative Research
Rolandic epilepsy-speech dyspraxia syndrome
rareA 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.
- Identifiers
- MONDO:0015587 Orphanet:163721
Subtypes
Projects
Including projects on subtypes.
No projects yet.