Epilepsy, Rolandic




Benign Childhood Epilepsy With Centro Temporal Spikes

Benign Childhood Epilepsy With Centro-Temporal Spikes

Benign Epilepsy Of Childhood With Centrotemporal Spikes

Benign Epilepsy With Centrotemporal Spikes

Benign Rolandic Epilepsy

Benign Rolandic Epilepsy of Childhood

Centralopathic Epilepsies

Centralopathic Epilepsy

Centrotemporal Epilepsies

Centrotemporal Epilepsy

Epilepsies, Centralopathic

Epilepsies, Centrotemporal

Epilepsies, Rolandic

Epilepsy, Benign Rolandic

Epilepsy, Centralopathic

Epilepsy, Centrotemporal

Epilepsy, Rolands

Epilepsy, Sylvian

Rolandic Epilepsies

Rolandic Epilepsy

Rolandic Epilepsy, Benign

Rolands Epilepsy

Sylvian Epilepsy

Temporal-Central Focal Epilepsy

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)