Genetics of Absence Epilepsy and Febrile Seizures

Authors

  • J Gordon Millichap Northwestern University Feinberg School of Medicine

DOI:

https://doi.org/10.15844/pedneurbriefs-17-1-11

Keywords:

Chromosome 5, Gene on Chromosomes, Absence Epilepsy

Abstract

In a large family with epilepsy studied at the University of Melbourne, Australia, FS in 18 children were inherited as autosomal dominant with 75% penetrance (GABA receptor subunit mutation on chromosome 5), and absence epilepsy in 8 required the GABA gene on chromosome 5 interacting with a possible further gene on chromosomes 10, 13, 14 and 15.

Published

2003-01-01

Issue

Section

Seizure Disorders