Chargement en cours...
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...
Enregistré dans:
| Auteurs principaux: | , , , , , , , |
|---|---|
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Hindawi Publishing Corporation
2013
|
| Sujets: | |
| Accès en ligne: | 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 |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|