Clinical outcomes and genotype-phenotype correlations in patients with complete and partial androgen insensitivity syndromes

PURPOSE: Androgen insensitivity syndrome (AIS) is a rare X-linked recessive disorder caused by unresponsiveness to androgens because of mutations in the AR gene. Here, we investigated the clinical outcomes and molecular spectrum of AR variants in patients with AIS attending a single academic center....

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Detalles Bibliográficos
Autores principales: Lee, Nae-yun, Kim, Ja Hye, Yoon, Ji-Hee, Hwang, Soojin, Kim, Gu-Hwan, Yoo, Han-Wook, Choi, Jin-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Pediatric Endocrinology 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10556439/
https://www.ncbi.nlm.nih.gov/pubmed/36731508
http://dx.doi.org/10.6065/apem.2244152.076

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10556439/
https://www.ncbi.nlm.nih.gov/pubmed/36731508
http://dx.doi.org/10.6065/apem.2244152.076

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