Bischoff Farideh, Simpson Joe Leigh
Baylor College of Medicine, Department of Obstetrics and Gynecology, 6550 Fannin, Suite 885, Houston, TX 77030, USA.
Ann N Y Acad Sci. 2004 Dec;1034:284-99. doi: 10.1196/annals.1335.030.
Endometriosis is a complex gynecologic disorder that has long been recognized as showing heritable tendencies, with recurrence risks of 5-7% for first-degree relatives. Familial and epidemiologic studies support that this disease is a genetic disorder of polygenic/multifactorial inheritance. The current investigational challenge is to determine the number and location of causative genes. Recent advances in molecular technology make identification and elucidation of these genes now possible. In this review, we update previous communications in which we also reviewed heritability studies supporting polygenic/multifactorial inheritance, discuss the scientific basis of genomewide strategies for identifying causative genes, and identify potential candidate genes.
子宫内膜异位症是一种复杂的妇科疾病,长期以来一直被认为具有遗传倾向,一级亲属的复发风险为5-7%。家族性和流行病学研究支持该疾病是一种多基因/多因素遗传的遗传性疾病。当前的研究挑战是确定致病基因的数量和位置。分子技术的最新进展使这些基因的识别和阐明成为可能。在本综述中,我们更新了之前的通讯,其中我们也回顾了支持多基因/多因素遗传的遗传力研究,讨论了识别致病基因的全基因组策略的科学依据,并确定了潜在的候选基因。