中国全科医学2013，Vol.16Issue(18)：2074-2075,2.DOI:10.3969/j.issn.1007-9572.2013.06.081
家族性偏瘫型偏头痛的遗传学研究进展
Progress of Genetic Research on Familial Hemiplegic Migraine
陈芳 1朱希芳 1孙涛 2徐文香 1张青青 1韩笑峰1
作者信息
- 1. 256600,山东省滨州市,滨州医学院附属医院神经科
- 2. 山东天宇医药有限公司
- 折叠
摘要
Abstract
Migraine is a common recurrent neurological disease,and about 6% of men and 18% of women in the general population are affected. In 2004 , the International Headache Society( HIS)divided the migraine into two classes: migraine with aura ( MA )and migraine without aura( MO ). Migraine is a disease with an obviously familial concentration. Its etiology is still unclear. Familial hemiplegic migraine( FHM ), being autosomal dominant inheritance, is the only one known as single gene inheritance. This paper reviews a variety of factors and candidate genes associated with FHM, and focuses on the known genes of CAC-NL1A4 and ATP1A2 in order to provide references for clinical physicians.
关键词
偏头痛/先兆偏头痛/遗传/综述Key words
Migraine disorders/ Migraine with aura/ Hereditary/ Review分类
医药卫生引用本文复制引用
陈芳,朱希芳,孙涛,徐文香,张青青,韩笑峰..家族性偏瘫型偏头痛的遗传学研究进展[J].中国全科医学,2013,16(18):2074-2075,2.
