FOXD1 mutations increase the risk of recurrent pregnancy loss.
What is it about?
About 1% of women suffer from recurrent pregnancy losses. The underlying genetics is ill-known. In this paper we report on variants of the FOXD1 gene that are associated with some cases of this disease.
Why is it important?
Sequencing of FOXD1 in women affected by Recurrent Pregnancy Losses could allow to diagnose the cause and to propose therapeutic solutions.
The following have contributed to this page: Dr Daniel Vaiman