Genetics and Genomics of Endometriosis

被引:45
作者
Hansen, Keith A. [1 ,3 ]
Eyster, Kathleen M. [2 ,3 ,4 ]
机构
[1] Univ S Dakota, Hlth Sci Ctr, Sanford Sch Med, Dept Obstet & Gynecol, Sioux Falls, SD 57107 USA
[2] Univ S Dakota, Sanford Sch Med, Div Basic Biomed Sci, Sioux Falls, SD 57107 USA
[3] Univ S Dakota, Sanford Sch Med, Dept Obstet & Gynecol, Vermillion, SD 57069 USA
[4] Univ S Dakota, Sanford Sch Med, Div Basic Biomed Sci, Vermillion, SD 57069 USA
关键词
endometriosis; genetics; familial; genomics; candidate genes; gene mapping; MICROARRAY ANALYSIS; EXPRESSION; POLYMORPHISMS; ASSOCIATION; RISK; HETEROZYGOSITY; GENES; WOMEN;
D O I
10.1097/GRF.0b013e3181db7ca1
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Endometriosis is a common cause of morbidity in women with an unknown etiology. Studies have demonstrated the familial nature of endometriosis and suggest that inheritance occurs in a polygenic/multifactorial fashion. Studies have attempted to define the gene or genes responsible for endometriosis through association or linkage studies with candidate genes or DNA mapping technology. A number of genomics studies have demonstrated significant alterations in gene expression in endometriosis. A more thorough understanding of the genetics and genomics of endometriosis will facilitate understanding the basic biology of the disease and open new inroads to diagnosis and treatment of this enigmatic condition.
引用
收藏
页码:403 / 412
页数:10
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