| Literature DB >> 10961632 |
Abstract
We report on a family having partial epilepsy with simple inheritance. The affected members commonly have aphasic episodes with secondary generalization; onset occurred either in adolescence or adulthood. Patients' response to medication has varied greatly. No neurological defects or decline in intelligence were found. The case represents another variety of rare familial partial epilepsy with neocortical epilepsy features.Entities:
Mesh:
Year: 2000 PMID: 10961632 DOI: 10.1111/j.1528-1157.2000.tb00290.x
Source DB: PubMed Journal: Epilepsia ISSN: 0013-9580 Impact factor: 5.864