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Glucocorticoid-Induced Osteoporosis in Children with 21-Hydroxylase Deficiency
21-Hydroxylase deficiency (21-OHD) is the most common cause of congenital adrenal hyperplasia (CAH), resulting from deletions or mutations of the P450 21-hydroxylase gene (CYP21A2). Children with 21-OHD need chronic glucocorticoid (cGC) therapy, both to replace congenital deficit in cortisol synthes...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi Publishing Corporation
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3581245/ https://ncbi.nlm.nih.gov/pubmed/23484098 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/250462 |
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