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.
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self-limited childhood occipital epilepsy
MONDO:0007558
Landau-Kleffner syndrome
MONDO:0009509
rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked
MONDO:0010388
rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
MONDO:0011970
perioral myoclonia with absences
MONDO:0015345
cryptogenic late-onset epileptic spasms
MONDO:0015585