Genetics of Primary Ovarian Insufficiency

被引:4
|
作者
Akande, Rukayat O. [1 ]
Ibrahim, Yetunde [2 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Sch Publ Hlth, Dept Management Policy & Community Hlth, Houston, TX 77030 USA
[2] Univ Texas Hlth Sci Ctr San Antonio, Dept Obstet & Gynecol, Div Reprod Endocrinol & Infertil, San Antonio, TX 78229 USA
来源
CLINICAL OBSTETRICS AND GYNECOLOGY | 2020年 / 63卷 / 04期
关键词
primary ovarian insufficiency; genes; syndromic; nonsyndromic; single nucleotide polymorphisms; fertility; FRAGILE-X PREMUTATION; BETA-SUBUNIT; MUTATIONAL ANALYSIS; CELL-SURVIVAL; YOUNG-WOMEN; FAILURE; FEMALE; AUTOPHAGY; REGION; HFM1;
D O I
10.1097/GRF.0000000000000575
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The diagnosis of primary ovarian insufficiency (POI) has untold effects on women and a better understanding alongside potential treatments are paramount to improve quality of life of these women. Various causes have been linked to the development of POI with genetics playing a key role. A better understanding of the genetics of POI could lead to earlier diagnosis and broaden fertility options. This chapter discusses previously known and more recently discovered genes that have been implicated in the development of POI. It explores the varying phenotypic expressions of some genes in different populations and areas for further research in the genetics of POI.
引用
收藏
页码:687 / 705
页数:19
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