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)

Descriptor ID	D019305
MeSH Number(s)	C10.228.140.490.360.280
Concept/Terms	Epilepsy, Rolandic Epilepsy, Rolandic Epilepsies, Rolandic Rolandic Epilepsies Rolandic Epilepsy Rolands Epilepsy Epilepsy, Rolands Sylvian Epilepsy Epilepsy, Sylvian Benign Rolandic Epilepsy Benign Rolandic Epilepsy Epilepsy, Benign Rolandic Rolandic Epilepsy, Benign BECTS Benign Childhood Epilepsy With Centro-Temporal Spikes Benign Childhood Epilepsy With Centro Temporal Spikes Benign Epilepsy Of Childhood With Centrotemporal Spikes Temporal-Central Focal Epilepsy Benign Rolandic Epilepsy of Childhood Centralopathic Epilepsy Centralopathic Epilepsies Epilepsies, Centralopathic Epilepsy, Centralopathic Centrotemporal Epilepsy Epilepsy, Centrotemporal Centrotemporal Epilepsies Epilepsies, Centrotemporal BCECTS Benign Epilepsy With Centrotemporal Spikes

Below are MeSH descriptors whose meaning is more general than "Epilepsy, Rolandic".

Below are MeSH descriptors whose meaning is related to "Epilepsy, Rolandic".

Below are MeSH descriptors whose meaning is more specific than "Epilepsy, Rolandic".