Congenital adrenal hyperplasia: Treatment and outcomes

Congenital adrenal hyperplasia (CAH) describes a group of autosomal recessive disorders where there is impairment of cortisol biosynthesis. CAH due to 21-hydroxylase deficiency accounts for 95% of cases and shows a wide range of clinical severity. Glucocorticoid and mineralocorticoid replacement the...

Descripción completa

Detalles Bibliográficos
Autores principales: Kamoun, Mahdi, Feki, Mouna Mnif, Sfar, Mohamed Habib, Abid, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830282/
https://www.ncbi.nlm.nih.gov/pubmed/24251136
http://dx.doi.org/10.4103/2230-8210.119491

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830282/
https://www.ncbi.nlm.nih.gov/pubmed/24251136
http://dx.doi.org/10.4103/2230-8210.119491

Ejemplares similares