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Glucocorticoid replacement regimens for treating congenital adrenal hyperplasia
BACKGROUND: Congenital adrenal hyperplasia (CAH) is an autosomal recessive condition which leads to glucocorticoid deficiency and is the most common cause of adrenal insufficiency in children. In over 90% of cases, 21‐hydroxylase enzyme deficiency is found which is caused by mutations in the 21‐hydr...
Gorde:
| Argitaratua izan da: | Cochrane Database Syst Rev |
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| Egile Nagusiak: | , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
John Wiley & Sons, Ltd
2020
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| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7081382/ https://ncbi.nlm.nih.gov/pubmed/32190901 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.CD012517.pub2 |
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