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Nonclassic Congenital Adrenal Hyperplasia
Nonclassic congenital adrenal hyperplasia (NCAH) due to P450c21 (21-hydroxylase deficiency) is a common autosomal recessive disorder. This disorder is due to mutations in the CYP21A2 gene which is located at chromosome 6p21. The clinical features predominantly reflect androgen excess rather than adr...
Gorde:
| Egile Nagusiak: | , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
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Hindawi Publishing Corporation
2010
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2910408/ https://ncbi.nlm.nih.gov/pubmed/20671993 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2010/625105 |
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