Epilepsy, Rolandic
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)
Year introduced: 1997
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Subheadings:
Tree Number(s): C10.228.140.490.360.280, C10.228.140.490.493.250
MeSH Unique ID: D019305
Entry Terms:
- Epilepsies, Rolandic
- Rolandic Epilepsies
- Rolandic Epilepsy
- Sylvian Epilepsy
- Epilepsy, Sylvian
- Rolands Epilepsy
- Epilepsy, Rolands
- Benign Rolandic Epilepsy
- Epilepsy, Benign Rolandic
- Rolandic Epilepsy, Benign
- Benign Rolandic Epilepsy of Childhood
- Epilepsy, Centrotemporal
- Centrotemporal Epilepsies
- Epilepsies, Centrotemporal
- Centralopathic Epilepsy
- Centralopathic Epilepsies
- Epilepsies, Centralopathic
- Epilepsy, Centralopathic
- BCECTS
- BECTS
- Benign Epilepsy With Centrotemporal Spikes
- Benign Epilepsy Of Childhood With Centrotemporal Spikes
- Temporal-Central Focal Epilepsy
- Epilepsies, Temporal-Central Focal
- Epilepsy, Temporal-Central Focal
- Focal Epilepsies, Temporal-Central
- Focal Epilepsy, Temporal-Central
- Temporal-Central Focal Epilepsies
- Temporal Central Focal Epilepsy
- Benign Childhood Epilepsy With Centro-Temporal Spikes
- Benign Childhood Epilepsy With Centro Temporal Spikes
- Centrotemporal Epilepsy
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