An autosomal dominant inherited partial epilepsy syndrome with onset between age 3 and 13 years. Seizures are characterized by PARESTHESIA and tonic or clonic activity of the lower face associated with drooling and dysarthria. In most cases, affected children are neurologically and developmentally normal. (From Epilepsia 1998 39;Suppl 4:S32-S41)
Also Known As:
Centrotemporal Epilepsy; Epilepsy, Rolandic; BCECTS; BECTS; Benign Rolandic Epilepsy; Centralopathic Epilepsy; Benign Childhood Epilepsy With Centro Temporal Spikes; Centralopathic Epilepsies; Centrotemporal Epilepsies; Epilepsies, Centralopathic; Epilepsies, Centrotemporal; Epilepsies, Rolandic; Epilepsy, Benign Rolandic; Epilepsy, Centralopathic; Epilepsy, Rolands; Epilepsy, Sylvian; Rolandic Epilepsies; Rolandic Epilepsy, Benign; Benign Childhood Epilepsy With Centro-Temporal Spikes; Benign Epilepsy With Centrotemporal Spikes; Benign Rolandic Epilepsy of Childhood; Epilepsy, Centrotemporal; Rolands Epilepsy; Sylvian Epilepsy