Rare and severe complications of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a case report
Open Access
- 6 February 2013
- journal article
- Published by Springer Science and Business Media LLC in Journal of Medical Case Reports
- Vol. 7 (1), 39
- https://doi.org/10.1186/1752-1947-7-39
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Two Adults with Adrenal Myelolipoma and 21-Hydroxylase DeficiencyCase Reports in Medicine, 2009
- Recent advances in diagnosis, treatment, and outcome of congenital adrenal hyperplasia due to 21-hydroxylase deficiencyReviews in Endocrine and Metabolic Disorders, 2007
- Congenital adrenal hyperplasia: Diagnostic advancesJournal of Inherited Metabolic Disease, 2007
- Bilateral adrenal myelolipoma associated with adrenogenital syndromeInternational Journal of Urology, 2006
- Testicular adrenal rest tumours in salt wasting congenital adrenal hyperplasia (in vivo and in vitro studies)The Journal of Steroid Biochemistry and Molecular Biology, 2005
- Congenital Adrenal HyperplasiaThe New England Journal of Medicine, 2003
- Future Directions in the Study and Management of Congenital Adrenal Hyperplasia due to 21-Hydroxylase DeficiencyAnnals of Internal Medicine, 2002
- Long Term Outcome in Adult Males with Classic Congenital Adrenal HyperplasiaJournal of Clinical Endocrinology & Metabolism, 2001
- Congenital Adrenal Hyperplasia due to 21-Hydroxylase DeficiencyEndocrine Reviews, 2000
- Adrenal Myelolipoma Associated with Congenital Adrenal 21-Hydroxylase Deficiency.Internal Medicine, 1992