Successful live birth in a woman with partial 17α-hydroxylase/17,20 lyase deficiency: a case report
Background17a-hydroxylase/17,20-lyase deficiency (17-OHD) is a rare form of congenital adrenal hyperplasia caused by mutations in the CYP17A1 gene, resulting in impaired activity of the corresponding enzymes. Its typical manifestations include hypertension, hypokalemia, and disorders of sexual devel...
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| Principais autores: | , , , , , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Frontiers Media S.A.
2026-07-01
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| 叢編: | Frontiers in Medicine |
| 主題: | |
| 在線閱讀: | https://www.frontiersin.org/articles/10.3389/fmed.2026.1883585/full |
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