Genetics of primary ovarian insufficiency: new developments and opportunities.

ABSTRACT:

Background

Primary ovarian insufficiency (POI) is characterized by marked heterogeneity, but with a significant genetic contribution. Identifying exact causative genes has been challenging, with many discoveries not replicated. It is timely to take stock of the field, outlining the progress made, framing the controversies and anticipating future directions in elucidating the genetics of POI.

Methods

A search for original articles published up to May 2015 was performed using PubMed and Google Scholar, identifying studies on the genetic etiology of POI. Studies were included if chromosomal analysis, candidate gene screening and a genome-wide study were conducted. Articles identified were restricted to English language full-text papers.

Results

Chromosomal abnormalities

SUBMITTER: Qin Y 

PROVIDER: S-EPMC4594617 | biostudies-literature | 2015 Nov-Dec

REPOSITORIES: biostudies-literature