A rare cause of hypertension in a healthy 2-year-old female: Answers
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s00467-012-2164-2.pdf
Reference16 articles.
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2. Biglieri EG (1979) Mechanisms establishing the mineralocorticoid hormone patterns in the 17 alpha-hydroxylase deficiency syndrome. J Steroid Biochem 11:653–657
3. Wang W, Fu JF, Gong FQ, Zhu WH, Shen Z (2011) Rare hypertension as a result of 17alpha-hydroxylase deficiency. J Pediatr Endocrinol Metab 24:333–337
4. Krone N, Arlt W (2009) Genetics of congenital adrenal hyperplasia. Best Pract Res Clin Endocrinol Metab 23:181–192
5. Costa-Santos M, Kater CE, Auchus RJ, Brazilian Congenital Adrenal Hyperplasia Multicenter Study Group (2004) Two prevalent CYP17 mutations and genotype-phenotype correlations in 24 Brazilian patients with 17-hydroxylase deficiency. J Clin Endocrinol Metab 89:49–60
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