A Summary of the Endocrine Society Clinical Practice Guidelines on Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency

Steroid 21-hydroxylase deficiency accounts for about 95% of cases of congenital adrenal hyperplasia (CAH). Newborns are currently being screened for the classical forms of this disease throughout the United States and in 12 other countries. As such, it seems important to develop the best practice gu...

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Bibliografische gegevens
Hoofdauteurs: Speiser, Phyllis W., Azziz, Ricardo, Baskin, Laurence S., Ghizzoni, Lucia, Hensle, Terry W., Merke, Deborah P., Meyer-Bahlburg, Heino F. L., Miller, Walter L., Montori, Victor M., Oberfield, Sharon E., Ritzen, Martin, White, Perrin C.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Hindawi Publishing Corporation 2010
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Commentary
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2963799/
https://ncbi.nlm.nih.gov/pubmed/20981249
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2010/494173
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