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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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Detalles Bibliográficos
Autores principales:	Ammar, Rasha, Ramadan, Ahmad
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2020
Materias:	Case Report
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

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