Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: A five-year retrospective study in the Children's Hospital of Damascus, Syria

Background: Congenital adrenal hyperplasia (CAH) is one of the most common inherited metabolic disorders. 21-hydroxylase deficiency is responsible for the majority of cases (90-95%) and considered the most common cause of genital ambiguity. There are no statistics concerning the prevalence of this d...

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Detalles Bibliográficos
Autores principales: Sheikh Alshabab, Lina Ibrahem, AlebrahIm, Assad, Kaddoura, Ahmad, Al-Fahoum, Sahar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bloomsbury Qatar Foundation Journals 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614327/
https://www.ncbi.nlm.nih.gov/pubmed/26535179
http://dx.doi.org/10.5339/qmj.2015.11

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614327/
https://www.ncbi.nlm.nih.gov/pubmed/26535179
http://dx.doi.org/10.5339/qmj.2015.11

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