Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency in a Tunisian family

Congenital adrenal hyperplasia refers to a group of rare genetic disorders affecting the adrenal glands. 21-hydroxylase deficiency is the most prevalent and the most studied cause while the remaining enzymatic defects are less common, accounting for less than 10% of cases. We herein described the cl...

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Detalles Bibliográficos
Autores principales: Elfekih, Hamza, Abdelkrim, Asma Ben, Marzouk, Hajer, Saad, Ghada, Gribaa, Moez, Hasni, Yosra, Maaroufi, Amel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7908330/
https://www.ncbi.nlm.nih.gov/pubmed/33708317
http://dx.doi.org/10.11604/pamj.2020.36.226.24270

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7908330/
https://www.ncbi.nlm.nih.gov/pubmed/33708317
http://dx.doi.org/10.11604/pamj.2020.36.226.24270

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