A child with hypertension and ambiguous genitalia – an uncommon variant of congenital adrenal hyperplasia: a case report

BACKGROUND: Deficiency in 11β-hydroxylase as a cause of congenital adrenal hyperplasia is uncommon. It should be considered in the differential diagnosis of hypertension with virilization in any prepubescent child. CASE PRESENTATION: A 12-year-old Asian boy from eastern Nepal presented with pain in...

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Detalles Bibliográficos
Autores principales: Pant, Vivek, Baral, Suman, Shrestha, Bishal, Tumbapo, Arjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481860/
https://www.ncbi.nlm.nih.gov/pubmed/28641572
http://dx.doi.org/10.1186/s13256-017-1341-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481860/
https://www.ncbi.nlm.nih.gov/pubmed/28641572
http://dx.doi.org/10.1186/s13256-017-1341-0

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