A rare, genetic, familial partial epilepsy disease characterized by focal seizures associated with prominent ictal auditory symptoms, and/or receptive aphasia, presenting in two or more family members and having a relatively benign evolution.
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familial sleep-related hypermotor epilepsy
MONDO:0000030
temporal lobe epilepsy
MONDO:0005115
self-limited epilepsy with centrotemporal spikes
MONDO:0007295
generalized epilepsy-paroxysmal dyskinesia syndrome
MONDO:0012276
autosomal dominant nocturnal frontal lobe epilepsy
MONDO:0020300
familial focal epilepsy with variable foci
MONDO:0020310