11β Hydroxylase Deficiency in a Child with Hypothyroidism: A Case Report
Congenital adrenal hyperplasia occurs due to enzymatic defects in the adrenocortical steroidogenesis. 11β hydroxylase deficiency is the second most common cause of congenital adrenal hyperplasia which presents with hypertension and features of androgen excess. Hypertension has also been found to ca...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Nepal Medical Association
2023-12-01
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| Series: | Journal of Nepal Medical Association |
| Subjects: | |
| Online Access: | https://www.jnma.com.np/jnma/index.php/jnma/article/view/8378 |