Congenital Adrenal Hyperplasia and Ehlers-Danlos Syndrome

Congenital adrenal hyperplasia (CAH) secondary to 21-hydroxylase deficiency is an autosomal recessive disorder. The 21-hydroxylase enzyme P450c21 is encoded by the CYP21A2 gene located on chromosome 6p21.33 within the HLA major histocompatibility complex. This locus also contains the CYP21A1P, a non...

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Detalles Bibliográficos
Autores principales: Marino, Roxana, Moresco, Angélica, Perez Garrido, Natalia, Ramirez, Pablo, Belgorosky, Alicia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8913572/
https://www.ncbi.nlm.nih.gov/pubmed/35282436
http://dx.doi.org/10.3389/fendo.2022.803226

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8913572/
https://www.ncbi.nlm.nih.gov/pubmed/35282436
http://dx.doi.org/10.3389/fendo.2022.803226

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