Cargando…
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...
Autores principales: | Pant, Vivek, Baral, Suman, Shrestha, Bishal, Tumbapo, Arjun |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
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 |
Ejemplares similares
-
MON-360 Genital Reconstruction for Ambiguous Genitalia: A Case Report on Congenital Adrenal Hyperplasia
por: Ching, Cheryl May, et al.
Publicado: (2019) -
Case report: Coexistence of Jacobs syndrome, congenital adrenal hyperplasia, and ambiguous genitalia in a male infant
por: Khan, Qaisar Ali, et al.
Publicado: (2023) -
Diabetic fetopathy associated with bilateral adrenal hyperplasia and ambiguous genitalia: a case report
por: Tantbirojn, Patou, et al.
Publicado: (2008) -
A rare variety of congenital adrenal hyperplasia with mosaic Klinefelter syndrome: a unique combination presenting with ambiguous genitalia and sexual precocity
por: Shehab, M A, et al.
Publicado: (2018) -
Nonvirilized Genitalia in 3 Female Newborns With the Salt-Wasting Congenital Adrenal Hyperplasia Phenotype
por: Yauch, Lauren, et al.
Publicado: (2020)