Premature ovarian insufficiency (POI) is defined as the loss of ovarian function in women under 40, and genetic factors may contribute to this condition, particularly in Turkey.
Researchers analyzed 86 cases of nonsyndromic POI and 26 control participants, focusing on cytogenetic abnormalities and known gene variants associated with POI.
They identified structural cytogenetic abnormalities in 4.6% of cases and an FMR1 premutation in 2.4%; however, the link to other premature ovarian insufficiency-related genes was weak, indicating that the novel gene variants discovered require further investigation to understand their potential role in POI.