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发作性睡病及其他主要睡眠障碍的遗传学

Genetics of narcolepsy and other major sleep disorders.

作者信息

Maret Stéphanie, Tafti Mehdi

机构信息

Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerand.

出版信息

Swiss Med Wkly. 2005 Nov 19;135(45-46):662-5. doi: 10.4414/smw.2005.11162.

Abstract

One third of the population is affected by a sleep disorder with a major social, medical, and economic impact. Although very little is known about the genetics of normal sleep, familial and twin studies indicate an important influence of genetic factors. Most sleep disorders run in families and in several of them the contribution of genetic factors is increasingly recognised. With recent advances in the genetics of narcolepsy and the role of the hypocretin/orexin system, the possibility that other gene defects may contribute to the pathophysiology of major sleep disorders is worth indepth investigation.

摘要

三分之一的人口受到睡眠障碍的影响,这具有重大的社会、医学和经济影响。尽管对正常睡眠的遗传学了解甚少,但家族研究和双生子研究表明遗传因素具有重要影响。大多数睡眠障碍在家族中具有遗传性,并且其中几种睡眠障碍中遗传因素的作用日益得到认可。随着发作性睡病遗传学及下丘脑分泌素/食欲素系统作用方面的最新进展,其他基因缺陷可能导致主要睡眠障碍病理生理学改变的可能性值得深入研究。

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