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多发性硬化症的遗传流行病学:一项调查

Genetic epidemiology of multiple sclerosis: a survey.

作者信息

Sadovnick A D

机构信息

Department of Medical Genetics, University of British Columbia, Vancouver, Canada.

出版信息

Ann Neurol. 1994 Dec;36 Suppl 2:S194-203. doi: 10.1002/ana.410360806.

Abstract

The possible role of genetic factors in the etiology of multiple sclerosis (MS) has been debated for over a century. It is now clear that genetic and environmental interactions must exist. It is likely that MS susceptibility is under the control of several genes encoded both within and outside the major histocompatibility complex (MHC). It is therefore unlikely that MS has a purely transmissible cause for these and other reasons, including the low concordance rate in dizygotic twins, low concordance rate in conjugal pairs, negative birth order in multiplex MS sibships, the relatively high rate of MS in second- and third-degree relatives of MS patients, and the identification of groups resistant to MS in otherwise high-risk areas.

摘要

遗传因素在多发性硬化症(MS)病因学中的可能作用已经争论了一个多世纪。现在很清楚,遗传和环境相互作用必然存在。MS易感性很可能受主要组织相容性复合体(MHC)内外编码的多个基因控制。因此,由于这些及其他原因,包括双卵双胞胎的低一致性率、配偶对的低一致性率、多发性MS同胞关系中的出生顺序为负、MS患者二级和三级亲属中相对较高的MS发病率,以及在其他高危地区发现对MS有抵抗力的群体,MS不太可能有纯粹的可遗传病因。

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