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Incidental diagnosis of 17 alpha-hydroxylase deficiency: a case report
A 17 alpha-hydroxylase deficiency (17OHD) is a rare form of congenital adrenal hyperplasia (CAH). In this article we discuss a case of 8-year-old girl presented with upper respiratory infection symptoms and a history of hospital admission of fatigue and dehydration. She was incidentally found to hav...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7720419/ https://www.ncbi.nlm.nih.gov/pubmed/33304598 http://dx.doi.org/10.1093/omcr/omaa108 |