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NONCLASSICAL 21-HYDROXYLASE DEFICIENCY PRESENTED AS ADDISON’S DISEASE AND BILATERAL ADRENAL INCIDENTALOMAS
BACKGROUND: 21-hydroxylase deficiency (21 OHD) is the most common form of congenital adrenal hyperplasia (CAH) and it has been widely described in the literature. Adrenocortical incidentalomas are unfrequently the presenting manifestations of CAH, especially in nonclassical form of 21 OHD (NC 21 OHD...
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| Publicado en: | Acta Endocrinol (Buchar) |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Acta Endocrinologica Foundation
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6516436/ https://ncbi.nlm.nih.gov/pubmed/31149180 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4183/aeb.2017.232 |
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