Abstract
A case of familial primary hyperaldosteronism in a 2-yr-old girl is presented. The unique feature of this case is that, as opposed to other familial cases, the patient′s hyperse-cretion of aldosterone could not be suppressed by glucocorticoids. Another interesting feature of this case was the persistent normokalemia in the face of definite hyperaldosteronism. © 1982 by The Endocrine Society.
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CITATION STYLE
Greco, R. G., Carroll, J. E., Morris, D. J., Grekin, R. J., & Melby, J. C. (1982). Familial Hyperaldosteronism, Not Suppressed by Dexamethasone. Journal of Clinical Endocrinology and Metabolism, 55(5), 1013–1016. https://doi.org/10.1210/jcem-55-5-1013
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