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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| Auteurs principaux: | , , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Frontiers Media S.A.
2022-02-01
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| Collection: | Frontiers in Endocrinology |
| Sujets: | |
| Accès en ligne: | https://www.frontiersin.org/articles/10.3389/fendo.2022.803226/full |
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