Coexistence of different phenotypes in a family with glucocorticoid-remediable aldosteronism
Author:
Publisher
Springer Science and Business Media LLC
Subject
Internal Medicine
Link
http://www.nature.com/articles/1001636.pdf
Reference22 articles.
1. Sutherland DJA, Ruse JL, Laidlaw JC . Hypertension, increased aldosterone secretion and low plasma renin activity relieved by dexamethasone. Can Med Assoc J 1966; 95: 1109–1119.
2. Dluhy RG, Lifton RF . Glucocorticoid-remediable aldosteronism. J Clin Endocrinol Metab 1999; 84: 4341–4344.
3. Stowasser M, Gordon RD . Primary aldosteronism: learning from the study of familial varieties. J Hypertens 2000; 18: 1165–1176.
4. Lifton RB et al. A chimaeric 11β-hydroxylase/aldosterone synthase gene causes glucocorticoid remediable aldosteronism and human hypertension. Nature 1992; 35: 262–265.
5. Mulatero P et al. Diagnosis of glucocorticoid-remediable aldosteronism in primary aldosteronism: aldosterone response to dexamethasone and long polymerase chain reaction for chimeric gene. J Clin Endocrinol Metab 1998; 83: 2573–2575.
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