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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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| Publicat a: | Pan Afr Med J |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The African Field Epidemiology Network
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7908330/ https://ncbi.nlm.nih.gov/pubmed/33708317 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2020.36.226.24270 |
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