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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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| Pubblicato in: | Horm Metab Res |
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| Autori principali: | , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2010
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| Soggetti: | |
| Accesso online: | 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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