A new locus for generalized epilepsy with febrile seizures plus maps to chromosome 2

被引:58
作者
Lopes-Cendes, I
Scheffer, IE
Berkovic, SF
Rousseau, M
Andermann, E
Rouleau, GA
机构
[1] McGill Univ, Montreal Gen Hosp, Res Inst, Ctr Res Neurosci, Montreal, PQ H3G 1A4, Canada
[2] McGill Univ, Montreal Neurol Hosp & Inst, Neurogenet Unit, Montreal, PQ H3G 1A4, Canada
[3] McGill Univ, Dept Neurol & Neurosurg, Montreal, PQ H3G 1A4, Canada
[4] McGill Univ, Dept Human Genet, Montreal, PQ H3G 1A4, Canada
[5] Univ Melbourne, Epilepsy Res Inst, Austin & Repatriat Med Ctr, Dept Med Neurol, Melbourne, Vic, Australia
[6] Royal Childrens Hosp, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
D O I
10.1086/302768
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Generalized epilepsy with febrile seizures plus (GEFS+) is a recently recognized but relatively common form of inherited childhood-onset epilepsy with heterogeneous epilepsy phenotypes. We genotyped 41 family members, including 21 affected individuals, to localize the gene causing epilepsy in a large family segregating an autosomal dominant form of GEFS+. A genomewide search examining 197 markers identified linkage of GEFS+ to chromosome 2, on the basis of an initial positive LOD score for marker D2S294 (Z = 4.4, recombination fraction [theta] = 0). A total of 24 markers were tested on chromosome 2q, to define the smallest candidate region for GEFS+. The highest two-point LOD score (Z(max) = 5.29; theta = 0) was obtained with marker D2S324. Critical recombination events mapped the GEFS+ gene to a 29-cM region flanked by markers D2S156 and D2S311, with the idiopathic generalized epilepsy locus thereby assigned to chromosome 2q23-q31. The existence of the heterogeneous epilepsy phenotypes in this kindred suggests that seizure predisposition determined by the GEFS+ gene on chromosome 2q could be modified by other genes and/or by environmental factors, to produce the different seizure types observed.
引用
收藏
页码:698 / 701
页数:4
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