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前庭性偏头痛发病机制的基因学研究进展

孙素芬 司楠楠 索利敏

中华耳科学杂志2018,Vol.16Issue(3):307-311,5.
中华耳科学杂志2018,Vol.16Issue(3):307-311,5.DOI:10.3969/j.issn.1672-2922.2018.03.010

前庭性偏头痛发病机制的基因学研究进展

Advances in Genetic Studies on the Pathogenesis of Vestibular Migraine

孙素芬 1司楠楠 1索利敏1

作者信息

  • 1. 山西医科大学第二医院耳鼻咽喉头颈外科
  • 折叠

摘要

Abstract

Vestibular Migraine (VM), a common clinical disease, is a benign recurrent vertigo that coexists with migraine, and recurrence of symptoms seriously affects the quality of life of patients. The diagnostic criteria of the VM become definite untill 2012 and rapidly become a new focus of research in the field of diagnosis and treatment. This arti-cle reviews the pathogenesis of VM, especially in genetics, in order to provide more evidences for diagnosis, treatment, prognosis and prevention of VM.

关键词

前庭性偏头痛/发病机制/基因

Key words

Vestibular Migraine/Pathogenesis/Gene

分类

医药卫生

引用本文复制引用

孙素芬,司楠楠,索利敏..前庭性偏头痛发病机制的基因学研究进展[J].中华耳科学杂志,2018,16(3):307-311,5.

基金项目

山西省回国留学人员科研资助项目(No:2017-118) Research Project Supported by Shanxi Scholarship Council of China. (No:2017-118 ) (No:2017-118)

中华耳科学杂志

OA北大核心CSCDCSTPCD

1672-2922

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