Aldosterone-to-Renin Ratio as a Marker for Disease Severity in 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia
Author:
Affiliation:
1. Department of Pediatrics (S.N., K.L.-S., R.C.W., M.I.N.), Adrenal Steroid Disorders Program, New York, New York 10029
2. Department of Community and Preventive Medicine (N.B.), Mount Sinai School of Medicine, New York, New York 10029
Publisher
The Endocrine Society
Subject
Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Link
http://academic.oup.com/jcem/article-pdf/92/1/137/11059263/jcem0137.pdf
Reference34 articles.
1. Steroid 21-hydroxylase deficiency: genotype may not predict phenotype.;Wilson;J Clin Endocrinol Metab,1995
2. Aldosterone excretion in normal children and in children with adrenal hyperplasia.;New;J Clin Invest,1966
3. Genotyping steroid 21-hydroxylase deficiency: hormonal reference data.;New;J Clin Endocrinol Metab,1983
4. An update of congenital adrenal hyperplasia.;New;Ann NY Acad Sci,2004
5. Aldosterone synthesis in salt-wasting congenital adrenal hyperplasia with complete absence of adrenal 21-hydroxylase.;Speiser;N Engl J Med,1991
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