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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...

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Bibliografski detalji
Izdano u:Oxf Med Case Reports
Glavni autori: Ammar, Rasha, Ramadan, Ahmad
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2020
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7720419/
https://ncbi.nlm.nih.gov/pubmed/33304598
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/omcr/omaa108
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