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Nonclassical Congenital Adrenal Hyperplasia and Pregnancy
Objective. The most common form of congenital adrenal hyperplasia (CAH) is 21-hydroxylase (21-OH) deficiency due to mutation of the CYP21A2 gene. Patients with nonclassical CAH (NC-CAH) are usually asymptomatic at birth and typically present in late childhood, adolescence, or adulthood with symptoms...
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| Vydáno v: | Case Rep Endocrinol |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Hindawi Publishing Corporation
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4618115/ https://ncbi.nlm.nih.gov/pubmed/26558116 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2015/296924 |
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