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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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Bibliografiske detaljer
Udgivet i:Acta Endocrinol (Buchar)
Main Authors: Meng, X., Yu, Y.
Format: Artigo
Sprog:Inglês
Udgivet: Acta Endocrinologica Foundation 2017
Fag:
Online adgang: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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