Nam Menke Marie, Strauss Jerome F
Virginia Commonwealth University Health System, Richmond, Virginia, USA.
Clin Obstet Gynecol. 2007 Mar;50(1):188-204. doi: 10.1097/GRF.0b013e3180305f7c.
Polycystic ovarian syndrome is a complex disorder with multiple factors affecting its etiology. Elucidation of specific genes and mode of inheritance remains a significant challenge. Linkage and association studies have resulted in over 50 candidate genes as a source of heritable predisposition; however, small sample sizes and failure to reproduce results have hindered efforts. In addition, low fecundity, lack of a male phenotype, and variation of diagnostic criteria represent unique challenges to discovery of polycystic ovarian syndrome genes. A concerted effort will be necessary to conclusively rule in or rule out candidate genes.
多囊卵巢综合征是一种复杂的疾病,有多种因素影响其病因。阐明特定基因和遗传模式仍然是一项重大挑战。连锁和关联研究已产生了50多个候选基因作为遗传易感性的来源;然而,样本量小和结果无法重复阻碍了相关研究。此外,低生育力、缺乏男性表型以及诊断标准的差异对多囊卵巢综合征基因的发现构成了独特的挑战。需要共同努力才能最终确定或排除候选基因。