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Epilepsy, Rolandic
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History note: | Epilepsy, Partial (1986-1996)X |
historyNote*: | 1997
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publicMeSHNote*: | 1997
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Scope note: | 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. The episodes tend to occur at night and may become secondarily generalized. In most cases, affected children are neurologically and developmentally normal. The electroencephalogram shows characteristic high-voltage sharp waves over the central temporal regions, which are more prominent during drowsiness and sleep. In general, seizures do not continue beyond mid-adolescence. (From Epilepsia 1998 39;Suppl 4:S32-S41)
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activeMeSHYear*: | |
dateCreated*: | 1996-06-13X |
dateEstablished*: | 1997-01-01X |
dateRevised*: | 1999-12-13X |
recordAuthorizer*: | agsX |
recordMaintainer*: | agsX |
recordOriginator*: | JLSX |
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Labels and equivalent concepts: | Rolandinen epilepsia (fi) XEpilepsia, Rolandinen (fi, replaced) Epilepsi, rolandisk (sv) Rolands Epilepsy (en, replaced) Sylvian Epilepsy (en, replaced) Epilepsy, Centrotemporal (en, replaced) Centralopathic Epilepsy (en, replaced) Benign Epilepsy, Childhood, Centrotemporal Spikes (en, replaced) Benign Rolandic Epilepsy (en, replaced) Benign Rolandic Epilepsy of Childhood (en, replaced) Benign Childhood Epilepsy With Centro-Temporal Spikes (en, replaced) |
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