Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD

OBJECTIVE: Androgen insensivity syndrome (AIS) and 5α-reductase deficiency (5α-RD) present with indistinguishable phenotypes among the 46,XY disorders of sexual development (DSD) that usually necessitate molecular analyses for the definitive diagnosis in the prepubertal period. The aim was to evalua...

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Detalles Bibliográficos
Autores principales: Akcan, Neşe, Uyguner, Oya, Baş, Firdevs, Altunoğlu, Umut, Toksoy, Güven, Karaman, Birsen, Avcı, Şahin, Yavaş Abalı, Zehra, Poyrazoğlu, Şükran, Aghayev, Agharza, Karaman, Volkan, Bundak, Rüveyde, Başaran, Seher, Darendeliler, Feyza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176093/
https://www.ncbi.nlm.nih.gov/pubmed/35135181
http://dx.doi.org/10.4274/jcrpe.galenos.2022.2021-9-19

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176093/
https://www.ncbi.nlm.nih.gov/pubmed/35135181
http://dx.doi.org/10.4274/jcrpe.galenos.2022.2021-9-19

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