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...

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Detalles Bibliográficos
Autores principales: Dehneh, Nada, Jarjour, Rami, Idelbi, Sahar, Alibrahem, Assad, Al Fahoum, Sahar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
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

Internet

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

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