Genetic basis of migraine.

S J Peroutka
{"title":"Genetic basis of migraine.","authors":"S J Peroutka","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Rapid technological advances in the field of molecular genetics are being applied successfully to the analysis of migraine. Specific mutations leading to an increased risk of rare forms of migraine have been identified in both mitochondrial DNA and a calcium channel gene. Association studies have demonstrated that polymorphic variations in serotonergic and dopaminergic genes may alter the clinical susceptibility to migraine. Massive amounts of additional genetic data relating to migraine will be generated in the next few years. These data are revolutionizing the diagnosis and management of migraine, a heretofore subjective clinical disorder.</p>","PeriodicalId":79395,"journal":{"name":"Clinical neuroscience (New York, N.Y.)","volume":"5 1","pages":"34-7"},"PeriodicalIF":0.0000,"publicationDate":"1998-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical neuroscience (New York, N.Y.)","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Rapid technological advances in the field of molecular genetics are being applied successfully to the analysis of migraine. Specific mutations leading to an increased risk of rare forms of migraine have been identified in both mitochondrial DNA and a calcium channel gene. Association studies have demonstrated that polymorphic variations in serotonergic and dopaminergic genes may alter the clinical susceptibility to migraine. Massive amounts of additional genetic data relating to migraine will be generated in the next few years. These data are revolutionizing the diagnosis and management of migraine, a heretofore subjective clinical disorder.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
偏头痛的遗传基础。
分子遗传学领域的快速技术进步正成功地应用于偏头痛的分析。在线粒体DNA和钙通道基因中发现了导致罕见偏头痛风险增加的特定突变。关联研究表明,血清素能和多巴胺能基因的多态性变异可能改变偏头痛的临床易感性。与偏头痛有关的大量额外基因数据将在未来几年内产生。这些数据是革命性的诊断和管理偏头痛,迄今主观的临床疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Migraine headaches: epidemiology and comorbidity. Cortical electrophysiology in migraine and possible pathogenetic implications. Serotonin receptors and the acute attack of migraine. Role of magnesium in the pathogenesis and treatment of migraines. Nitric oxide theory of migraine.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1