Genetic basis of migraine.

S J Peroutka
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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.

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。
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