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...
| Main Authors: | , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
The Pan African Medical Journal
2020-07-01
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| Series: | The Pan African Medical Journal |
| Subjects: | |
| Online Access: |
https://www.panafrican-med-journal.com/content/article/36/226/pdf/226.pdf
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