Abstract
We describe the clinical and neurophysiological features of 14 non-familial cases of Idiopathic Lateral Temporal Epilepsy. Although the evolution may be variable, a group of patients may be identified with a phenotype fully resembling Autosomal Dominant Lateral Temporal Epilepsy. The relative paucity of secondarily generalised tonic-clonic seizures may distinguish clinically sporadic from familial cases.
Translated title of the contribution | Idiopathic lateral temporal epilepsy: An adult, benign, genetically related form of epilepsy? |
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Original language | Italian |
Pages (from-to) | 109-110 |
Number of pages | 2 |
Journal | Bollettino - Lega Italiana contro l'Epilessia |
Issue number | 118 |
Publication status | Published - Oct 2002 |
ASJC Scopus subject areas
- Clinical Neurology