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Updated: Sep 6, 2025

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Homozygous missense variants in BMPR15 can result in primary ovarian insufficiency
Leigh A M Demain1, Kay Metcalfe1, Eline Boetje2
1Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester Manchester, UK; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust Manchester, UK.
Research Question:
Does a genetic condition underlie the diagnosis of primary ovarian insufficiency (POI) in a 13-year-old girl with primary amenorrhoea?
Design:
A case report of a next-generation sequencing panel of 24 genes associated with syndromal and non-syndromal POI was conducted.
Results:
A homozygous missense variant c.1076C>T, p.(Pro359Leu) in BMP15 was identified.
Conclusions:
The biallelic variant c.1076C >T, p.(Pro359Leu) in BMP15 is associated with primary ovarian failure.
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