Two novel AMHR2 gene variants in monozygotic twins with persistent Müllerian duct syndrome: A case report and functional study

Two novel AMHR2 gene variants in monozygotic twins with persistent Müllerian duct syndrome: A case report and functional study

Abstract Background Persistent Müllerian duct syndrome (PMDS) is an autosomal recessive congenital abnormality in which Müllerian derivatives, uterus, cervix, upper two‐thirds of the vagina, and fallopian tubes persist in otherwise normally virilized males. Mutations in anti‐Müllerian hormone (AMH)...

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Bibliographic Details
Main Authors: Hong Chen, Peng Lin, Xin Yuan, Ruimin Chen
Format: Article
Language:English
Published: Wiley 2022-08-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
AMH
AMHR2 gene
persistent Müllerian duct syndrome
variants
Online Access:https://doi.org/10.1002/mgg3.1999

Internet

https://doi.org/10.1002/mgg3.1999

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