Cargando…
Syrian females with congenital adrenal hyperplasia: a case series
BACKGROUND: One of the most common types of congenital adrenal hyperplasia is an autosomal recessive disorder with 21-hydroxylase deficiency. The classical form, defined by cortisol insufficiency, is accompanied by prenatal androgen excess causing variable masculinization degrees of external genital...
Autores principales: | Dehneh, Nada, Jarjour, Rami, Idelbi, Sahar, Alibrahem, Assad, Al Fahoum, Sahar |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9569117/ https://www.ncbi.nlm.nih.gov/pubmed/36242011 http://dx.doi.org/10.1186/s13256-022-03609-y |
Ejemplares similares
-
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: A five-year retrospective study in the Children's Hospital of Damascus, Syria
por: Sheikh Alshabab, Lina Ibrahem, et al.
Publicado: (2015) -
Case Report of an Adult Female with Neglected Congenital Adrenal Hyperplasia (CAH)
por: Krishnan, Gayathri Devi, et al.
Publicado: (2018) -
Giant Bilateral Adrenal Myelolipoma with Congenital Adrenal Hyperplasia
por: Al-Bahri, S., et al.
Publicado: (2014) -
Editorial: Management of Females with Congenital Adrenal Hyperplasia
por: González, Ricardo, et al.
Publicado: (2017) -
A Case of Congenital Lipoid Adrenal Hyperplasia
por: Hashemipour, Mahin, et al.
Publicado: (2012)