PT - JOURNAL ARTICLE AU - R H Wallace AU - S F Berkovic AU - R A Howell AU - G R Sutherland AU - J C Mulley TI - Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21. AID - 10.1136/jmg.33.4.308 DP - 1996 Apr 01 TA - Journal of Medical Genetics PG - 308--312 VI - 33 IP - 4 4099 - http://jmg.bmj.com/content/33/4/308.short 4100 - http://jmg.bmj.com/content/33/4/308.full SO - J Med Genet1996 Apr 01; 33 AB - Febrile convulsions affect 2 to 5% of all children under the age of 5 years. These convulsions probably have a variety of causes, but a genetic component has long been recognised. A large and remarkable family is described in which febrile convulsions appear to result from autosomal dominant inheritance at a single major locus. A gene for febrile convulsions was excluded from regions of previously mapped epilepsy genes and extension of exclusion mapping, using microsatellite markers, to the entire genome implied that a locus on chromosome 8q13-21 may be involved. Linkage analysis of markers on chromosome 8 gave a multipoint lod score of 3.40, maximised over different values of penetrance and phenocopy rate, for linkage between the gene for febrile convulsions and the region flanked by markers D8S553 and D8S279. This lod score was calculated assuming the disease has a penetrance of 60% and a phenocopy rate of 3%. Although there was no indication of linkage other than to markers on chromosome 8, linkage remains suggestive rather than significant because of the maximisation procedure applied. The support for linkage involving a major gene, as opposed to an alternative hypothesis of a complex inheritance pattern, relied upon the assumption of low penetrance.