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Adrenomedullary Function in Patients with Nonclassic Congenital Adrenal Hyperplasia
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is classifi ed into three types based on disease severity: classic saltwasting, classic simple virilizing, and nonclassic. Adrenomedullary dysplasia and epinephrine deficiency have been described in classic CAH, resulting in gluco...
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| Vydáno v: | Horm Metab Res |
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| Hlavní autoři: | , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2010
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7473418/ https://ncbi.nlm.nih.gov/pubmed/20446239 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0030-1253385 |
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