Autosomal dominant partial epilepsy with auditory features: defining the phenotype
- PMID: 10851389
- PMCID: PMC2659636
- DOI: 10.1212/wnl.54.11.2173
Autosomal dominant partial epilepsy with auditory features: defining the phenotype
Abstract
The authors previously reported linkage to chromosome 10q22-24 for autosomal dominant partial epilepsy with auditory features. This study describes seizure semiology in the original linkage family in further detail. Auditory hallucinations were most common, but other sensory symptoms (visual, olfactory, vertiginous, and cephalic) were also reported. Autonomic, psychic, and motor symptoms were less common. The clinical semiology points to a lateral temporal seizure origin. Auditory hallucinations, the most striking clinical feature, are useful for identifying new families with this synome.
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