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Decreased Adrenomedullary Function in Infants With Classical Congenital Adrenal Hyperplasia
CONTEXT: Classical congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency can cause life-threatening adrenal crises as well as severe hypoglycemia, especially in very young children. Studies of CAH patients 4 years old or older have found abnormal morphology and function of the adrena...
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Endocrine Society
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4121032/ https://ncbi.nlm.nih.gov/pubmed/24878051 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2014-1274 |
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