Clinical Features of Unrecognized Congenital Adrenal Hyperplasia Due to 17α-hydroxylase Deficiency Since Adolescence: A Case Report

The majority of patients with congenital adrenal hyperplasia (CAH) present with a deficiency of 21-hydroxylase or 11-beta-hydroxylase, which account for 90% and 7% of cases, respectively. However, CAH due to 17α-hydroxylase deficiency (17OHD) is an extremely rare form of CAH (<1% of all CAH cases...

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Detalles Bibliográficos
Autores principales: Rashmi, KG, Ravichandran, Lavanya, Roy, Ayan, Naik, Dukhabandhu, Kamalanathan, Sadishkumar, Sahoo, Jayaprakash, Chapla, Aaron, Thomas, Nihal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Journal of the ASEAN Federation of Endocrine Societies 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10692439/
https://www.ncbi.nlm.nih.gov/pubmed/38045661
http://dx.doi.org/10.15605/jafes.038.02.08

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10692439/
https://www.ncbi.nlm.nih.gov/pubmed/38045661
http://dx.doi.org/10.15605/jafes.038.02.08

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