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Duration of Suppression of Adrenal Steroids after Glucocorticoid Administration

Hydrocortisone has long been the treatment of choice for congenital adrenal hyperplasia (CAH). However, treatment with this medication remains problematic. Patients with 21-hydroxylase deficiency CAH have significant diurnal variation in the secretion of 17-hydroxyprogesterone (17OHP). When consider...

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Autores principales: Fuqua, John S., Rotenstein, Deborah, Lee, Peter A.
Formato: Artigo
Lenguaje:Inglês
Publicado: Hindawi Publishing Corporation 2010
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2850127/
https://ncbi.nlm.nih.gov/pubmed/20379352
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2010/712549
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