A novel mutation (L250V) in the presenilin 1 gene in a Japanese familial Alzheimer's disease with myoclonus and generalized convulsion

被引:19
作者
Furuya, H [1 ]
Yasuda, M
Terasawa, K
Tanaka, K
Murai, H
Kira, J
Ohyagi, Y
机构
[1] Kyushu Univ, Grad Sch Med Sci, Inst Neurol, Dept Neurol, Fukuoka 8128582, Japan
[2] Hyogo Inst Aging Brain & Cognit Disorders, Himeji, Hyogo 6700981, Japan
[3] Terasawa Hosp, Fukuoka 8150084, Japan
[4] Fukuoka Red Cross Hosp, Dept Psychiat, Fukuoka 8158555, Japan
关键词
familial Alzheimer's disease; presenilin; 1; myoclonus; Japanese pedigree; tonic-clonic seizure;
D O I
10.1016/S0022-510X(02)00466-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
This study reports a novel presenilin 1 (PSI) gene mutation in a Japanese family with Alzheimer's disease (AD). Two patients developed progressive memory disorder with disorientation around 50 years of age and showed myoclonus with frequent tonic-clonic seizures several years later. Direct sequencing of the proband's PS1 gene revealed a novel mis-sense mutation (leucine-to-valine at residue 250 (L250V)). This mutation was found in both patients, but not in a normal family member or normal Japanese control subjects. Thus, L250V is a novel PS1 gene mutation responsible for familial AD (FAD) in Japan. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:75 / 77
页数:3
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