Rolandic epilepsy-speech dyspraxia syndrome
MONDO:0015587A 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.
9 clinical trials for this condition and its sub-types, 0 tagged with Rolandic epilepsy-speech dyspraxia syndrome itself.
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