Familial hyperreninemic hypoaldosteronism type 2

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Synonyms and keywords: Aldosterone synthase deficiency unlinked to CYP11B2; aldosterone synthase deficiency unlinked to the aldosterone synthase gene; FHHA2.

Overview

Familial hyperreninemic hypoaldosteronism type 2 is a very rare genetic disorder which results in a deficiency of aldosterone. The condition can be severe enough to cause infant death unless the patient is diagnosed and treated.