Identification of <i>AMH</i> and <i>AMHR2</i> Variants Led to the Diagnosis of Persistent Müllerian Duct Syndrome in Three Cases
Persistent Müllerian duct syndrome (PMDS) is a rare autosomal recessive disorder of sexual development in males, defined by the presence of Müllerian remnants with otherwise normal sexual differentiation. Mutations in anti-Müllerian hormone (<i>AMH</i>) and AMH receptor type 2 (<i>...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2022-01-01
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| Series: | Genes |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2073-4425/13/1/159 |