| Literature DB >> 7906762 |
I E Scheffer1, K P Bhatia, I Lopes-Cendes, D R Fish, C D Marsden, F Andermann, E Andermann, R Desbiens, F Cendes, J I Manson.
Abstract
We describe a distinctive epilepsy syndrome in six families, which is the first partial epilepsy syndrome to follow single gene inheritance. The predominant seizure pattern had frontal lobe seizure semiology with clusters of brief motor attacks occurring in sleep. Onset was usually in childhood, often persisting through adult life. Misdiagnosis as night terrors, nightmares, hysteria, or paroxysmal nocturnal dystonia was common, and the inheritance pattern was often not appreciated. This autosomal dominant epilepsy syndrome is ideal for identification of partial epilepsy genes.Entities:
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Year: 1994 PMID: 7906762 DOI: 10.1016/s0140-6736(94)91463-x
Source DB: PubMed Journal: Lancet ISSN: 0140-6736 Impact factor: 79.321