Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/7051
Citations
Scopus Web of Science® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.authorMarini, C.en
dc.contributor.authorHarkin, L.en
dc.contributor.authorWallace, R.en
dc.contributor.authorMulley, J.en
dc.contributor.authorScheffer, I.en
dc.contributor.authorBerkovic, S.en
dc.date.issued2003en
dc.identifier.citationBrain, 2003; 126(1):230-240en
dc.identifier.issn0006-8950en
dc.identifier.issn1460-2156en
dc.identifier.urihttp://hdl.handle.net/2440/7051-
dc.descriptionCopyright © 2003 Guarantors of Brainen
dc.description.abstractAlthough several genes for idiopathic epilepsies from families with simple Mendelian inheritance have been found, genes for the common idiopathic generalized epilepsies, where inheritance is complex, presently are elusive. We studied a large family with epilepsy where the two main phenotypes were childhood absence epilepsy (CAE) and febrile seizures (FS), which offered a special opportunity to identify epilepsy genes. A total of 35 family members had seizures over four generations. The phenotypes comprised typical CAE (eight individuals); FS alone (15), febrile seizures plus (FS+) (three); myoclonic astatic epilepsy (two); generalized epilepsy with tonic±clonic seizures alone (one); partial epilepsy (one); and unclassi®ed epilepsy despite evaluation (two). In three remaining individuals, no information was available. FS were inherited in an autosomal dominant fashion with 75% penetrance. The inheritance of CAE in this family was not simple Mendelian, but suggestive of complex inheritance with the involvement of at least two genes. A GABAA receptor g2 subunit gene mutation on chromosome 5 segregated with FS, FS+ and CAE, and also occurred in individuals with the other phenotypes. The clinical and molecular data suggest that the GABAA receptor subunit mutation alone can account for the FS phenotype. An interaction of this gene with another gene or genes is required for the CAE phenotype in this family. Linkage analysis for a putative second gene contributing to the CAE phenotype suggested possible loci on chromosomes 10, 13, 14 and 15. Examination of these loci in other absence pedigrees is warranted.en
dc.description.statementofresponsibilityCarla Marini, Louise A. Harkin, Robyn H. Wallace, John C. Mulley, Ingrid E. Scheffer and Samuel F. Berkovicen
dc.language.isoenen
dc.publisherOxford Univ Pressen
dc.subjectchildhood absence epilepsy; epilepsy; GABAA receptor; genetics; linkage analysisen
dc.titleChildhood absence epilepsy and febrile seizures: a family with a GABAA receptor mutationen
dc.typeJournal articleen
dc.identifier.rmid0020031325en
dc.identifier.doi10.1093/brain/awg018en
dc.identifier.pubid58254-
pubs.library.collectionPaediatrics publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
Appears in Collections:Paediatrics publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.