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本文引用的文献

1
Identification of a new locus for generalized epilepsy with febrile seizures plus (GEFS+) on chromosome 2q24-q33.在2号染色体2q24-q33区域发现热性惊厥附加症伴发的全身性癫痫(GEFS+)的一个新基因座。
Am J Hum Genet. 1999 Nov;65(5):1396-400. doi: 10.1086/302621.
2
A locus for febrile seizures (FEB3) maps to chromosome 2q23-24.热性惊厥的一个基因座(FEB3)定位于2号染色体的2q23-24区域。
Ann Neurol. 1999 Oct;46(4):671-8. doi: 10.1002/1531-8249(199910)46:4<671::aid-ana20>3.0.co;2-5.
3
A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33.伴有热性惊厥附加症的家族性全身性癫痫的第二个基因座定位于2号染色体的2q21-q33区域。
Am J Hum Genet. 1999 Oct;65(4):1078-85. doi: 10.1086/302593.
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Genetics of the epilepsies.癫痫的遗传学
Curr Opin Neurol. 1999 Apr;12(2):177-82. doi: 10.1097/00019052-199904000-00008.
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Generalized epilepsy with febrile seizures plus: a common childhood-onset genetic epilepsy syndrome.伴有热性惊厥附加症的全身性癫痫:一种常见的儿童期起病的遗传性癫痫综合征。
Ann Neurol. 1999 Jan;45(1):75-81. doi: 10.1002/1531-8249(199901)45:1<75::aid-art13>3.0.co;2-w.
6
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.热性惊厥和与钠离子通道β1亚基基因SCN1B突变相关的全身性癫痫。
Nat Genet. 1998 Aug;19(4):366-70. doi: 10.1038/1252.
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A potassium channel mutation in neonatal human epilepsy.新生儿人类癫痫中的一种钾通道突变。
Science. 1998 Jan 16;279(5349):403-6. doi: 10.1126/science.279.5349.403.
8
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.一个新的钾通道基因KCNQ2在新生儿遗传性癫痫中发生突变。
Nat Genet. 1998 Jan;18(1):25-9. doi: 10.1038/ng0198-25.
9
Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes.伴有热性惊厥附加症的全面性癫痫。一种具有异质性临床表型的遗传性疾病。
Brain. 1997 Mar;120 ( Pt 3):479-90. doi: 10.1093/brain/120.3.479.
10
Incidence of epilepsy and unprovoked seizures in Rochester, Minnesota: 1935-1984.明尼苏达州罗切斯特市癫痫和特发性癫痫发作的发病率:1935 - 1984年
Epilepsia. 1993 May-Jun;34(3):453-68. doi: 10.1111/j.1528-1157.1993.tb02586.x.

伴有热性惊厥附加症的全身性癫痫的一个新基因座定位于2号染色体。

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

作者信息

Lopes-Cendes I, Scheffer I E, Berkovic S F, Rousseau M, Andermann E, Rouleau G A

机构信息

Centre for Research in Neuroscience, The Montreal General Hospital Research Institute, Montreal Neurological Institute and Hospital, Montreal, Quebec, Canada.

出版信息

Am J Hum Genet. 2000 Feb;66(2):698-701. doi: 10.1086/302768.

DOI:10.1086/302768
PMID:10677328
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1288121/
Abstract

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 [straight 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 (Zmax=5.29; straight 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.

摘要

伴有热性惊厥附加症的全身性癫痫(GEFS+)是一种最近才被认识但相对常见的遗传性儿童期癫痫,具有异质性癫痫表型。我们对41名家庭成员进行了基因分型,其中包括21名受影响个体,以在一个分离常染色体显性形式GEFS+的大家庭中定位导致癫痫的基因。一项全基因组搜索检查了197个标记,基于标记D2S294的初始阳性LOD评分(Z = 4.4,重组率[直θ]= 0),确定GEFS+与2号染色体连锁。在2号染色体长臂上共测试了24个标记,以确定GEFS+的最小候选区域。标记D2S324获得了最高的两点LOD评分(Zmax = 5.29;直θ = 0)。关键的重组事件将GEFS+基因定位到一个29厘摩的区域,该区域两侧是标记D2S156和D2S311,特发性全身性癫痫位点因此被定位到2号染色体长臂2区3带至3区1带。这个家系中异质性癫痫表型的存在表明,2号染色体长臂上由GEFS+基因决定的癫痫易感性可能会被其他基因和/或环境因素改变,从而产生所观察到的不同癫痫类型。