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Hypoglycemia during acute illness in children with classic congenital adrenal hyperplasia
Congenital adrenal hyperplasia (CAH) describes a group of genetic, autosomal recessive conditions, where there is a block in cortisol biosynthesis. Approximately 95 percent of cases are due to 21-hydroxylase deficiency, which is discussed in this article. Patients with the severe or classic form of...
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| Hoofdauteurs: | , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2008
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2819226/ https://ncbi.nlm.nih.gov/pubmed/20117671 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.pedn.2008.06.003 |
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