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.
机构:
Erasmus MC, Dept Obstet & Gynecol, Div Reprod Med, POB 2040, NL-3000 CA Rotterdam, NetherlandsErasmus MC, Dept Obstet & Gynecol, Div Reprod Med, POB 2040, NL-3000 CA Rotterdam, Netherlands
机构:
NICHHD, Integrat Reprod Med Unit, Intramural Res Program Reprod & Adult Endocrinol, NIH,CRC, Bethesda, MD 20892 USANICHHD, Integrat Reprod Med Unit, Intramural Res Program Reprod & Adult Endocrinol, NIH,CRC, Bethesda, MD 20892 USA
Nelson, Lawrence M.
NEW ENGLAND JOURNAL OF MEDICINE,
2009,
360
(06):
: 606
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614
机构:
North Shore Private Hosp, Med Suites,Westbourne St, St Leonards, NSW 2065, Australia
Univ Sydney, Dept Obstet & Gynecol, St Leonards, NSW, AustraliaNorth Shore Private Hosp, Med Suites,Westbourne St, St Leonards, NSW 2065, Australia
Baber, Rodney J.
Kwik, Michele
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机构:
Univ Sydney, Dept Obstet & Gynecol, St Leonards, NSW, Australia
IVFAustralia, Greenwich, NSW 2065, AustraliaNorth Shore Private Hosp, Med Suites,Westbourne St, St Leonards, NSW 2065, Australia
Kwik, Michele
CURRENT OBSTETRICS AND GYNECOLOGY REPORTS,
2014,
3
(04):
: 223
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231