4.0 Article

The genetic basis of premature ovarian failure

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Publisher

WILEY
DOI: 10.1111/j.1479-828X.2006.00585.x

Keywords

candidate gene; FOXL2; genetic disorder; inhibin; premature ovarian failure

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Premature ovarian failure (POF) is a common condition, affecting approximately 1:100 women. It is characterised by amenorrhea, hypoestrogenism, and elevated gonadotrophin levels in women under the age of 40. It is often an unexpected and distressing diagnosis, which coincides with infertility and menopausal symptoms. There is a well recognised genetic basis to the development of POF. Our laboratory has identified several candidate genes associated with POF.

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