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)
推出的年份: 1997
树号: C10.228.140.490.360.280, C10.228.140.490.493.250
MeSH 单一 ID: D019305
进入的组:
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
Centrotemporal Epilepsy
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 Epilepsy
Temporal-Central Focal Epilepsies
Benign Childhood Epilepsy With Centro-Temporal Spikes
Benign Childhood Epilepsy With Centro Temporal Spikes
BCECTS
早前的内容:
Epilepsy, Partial (1986-1996)
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