A Novel Mutation of AMHR2 in Two Siblings with Persistent Müllerian Duct Syndrome

Persistent Müllerian Duct syndrome (PMDS) develops due to deficiency of anti-Müllerian hormone (AMH) or insensitivity of target organs to AMH in individuals with 46,XY karyotype. PMDS is characterized by normal male phenotype of external genitals, associated with persistence of Müllerian structures....

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Detalles Bibliográficos
Autores principales: Unal, Edip, Yıldırım, Ruken, Tekin, Suat, Demir, Vasfiye, Onay, Hüseyin, Haspolat, Yusuf Kenan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280330/
https://www.ncbi.nlm.nih.gov/pubmed/29687786
http://dx.doi.org/10.4274/jcrpe.0013

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280330/
https://www.ncbi.nlm.nih.gov/pubmed/29687786
http://dx.doi.org/10.4274/jcrpe.0013

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