Abstract
We describe the occurrence of primary hyperaldosteronism in two sisters. Although this is only the second published report of familial Conn's syndrome, it does have implications for the relatives of patients with Conn's syndrome and these are discussed.
Full text
PDF

Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- CONN J. W. Presidential address. I. Painting background. II. Primary aldosteronism, a new clinical syndrome. J Lab Clin Med. 1955 Jan;45(1):3–17. [PubMed] [Google Scholar]
- Greco R. G., Carroll J. E., Morris D. J., Grekin R. J., Melby J. C. Familial hyperaldosteronism, not suppressed by dexamethasone. J Clin Endocrinol Metab. 1982 Nov;55(5):1013–1016. doi: 10.1210/jcem-55-5-1013. [DOI] [PubMed] [Google Scholar]
- Irony I., Kater C. E., Biglieri E. G., Shackleton C. H. Correctable subsets of primary aldosteronism. Primary adrenal hyperplasia and renin responsive adenoma. Am J Hypertens. 1990 Jul;3(7):576–582. doi: 10.1093/ajh/3.7.576. [DOI] [PubMed] [Google Scholar]
- Stowasser M., Gordon R. D., Tunny T. J., Klemm S. A., Finn W. L., Krek A. L. Primary aldosteronism: implications of a new familial variety. J Hypertens Suppl. 1991 Dec;9(6):S264–S265. [PubMed] [Google Scholar]
