Journal article
Premature Ovarian Insufficiency: New Perspectives On Genetic Cause And Phenotypic Spectrum
EJ Tucker, SR Grover, A Bachelot, P Touraine, AH Sinclair
Endocrine Reviews | ENDOCRINE SOC | Published : 2016
DOI: 10.1210/er.2016-1047
Abstract
Premature ovarian insufficiency (POI) is one form of female infertility, defined by loss of ovarian activity before the age of 40 and characterized by amenorrhea (primary or secondary) with raised gonadotropins and low estradiol. POI affects up to one in 100 females, including one in 1000 before the age of 30. Substantial evidence suggests a genetic basis for POI; however, the majority of cases remain unexplained, indicating that genes likely to be associated with this condition are yet to be discovered. This review discusses the current knowledge of the genetic basis of POI. We highlight genes typically known to cause syndromic POI that can be responsible for isolated POI. The role of mouse..
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Awarded by National Health and Medical Research Council
Funding Acknowledgements
This work was supported by a Peter Doherty Early Career Fellowship (1054432; to E.J.T.), a National Health and Medical Research Council program grant (1074258; to A.H.S.), a fellowship (1062854; to A.H.S.) from the Australian National Health and Medical Research Council, and the Victorian Government's Operational Infrastructure Support Program.