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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Hlavní autoři: Kim, Mimi S., Ryabets-Lienhard, Anna, Bali, Bhavna, Lane, Christianne J., Park, Ashley H., Hall, Sandra, Geffner, Mitchell E.
Médium: Artigo
Jazyk:Inglês
Vydáno: Endocrine Society 2014
Témata:
JCEM Online: Advances in Genetics
On-line přístup: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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