Article

Two Novel AMHR2 Gene Variants in Monozygotic Twins with Persistent Müllerian Duct Syndrome

2021-08-03

Abstract excerpt

<title>Abstract</title> <p><bold>Background:</bold> Persistent müllerian duct syndrome (PMDS) is an autosomal recessive congenital abnormality for which müllerian derivatives, uterus, cervix, upper 2/3 vagina and fallopian tubes, persist in an otherwise normally virilized males. Mutations in the <italic>AMH</italic> gene and <italic>AMHR2</italic> gene have been identified as causative. However, there has been no...

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Literature Corpus work: 174af116-241a-5ec6-9ae4-4bed5ec70e65
DOI: 10.21203/rs.3.rs-728396/v1

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