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Recommendations for Treatment of Nonclassic Congenital Adrenal Hyperplasia (NCCAH): an Update
Congenital adrenal hyperplasia (CAH) is a family of autosomal recessive disorders. 21-hydroxylase deficiency, in which there are mutations in CYP21A2 (the gene encoding the adrenal 21-hydroxylase enzyme), is the most common form (90%) of CAH. In classic CAH there is impaired cortisol production with...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3638754/ https://ncbi.nlm.nih.gov/pubmed/22186144 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.steroids.2011.12.009 |
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