Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Familial hyperaldosteronism
Glucocorticoid-remediable aldosteronism
Familial hyperaldosteronism type I (FH-I) is a rare heritable, glucocorticoid remediable form of primary aldosteronism (PA) characterized by early-onset hypertension, hyperaldosteronism, variable hypokalemia, low plasma renin activity (PRA), and abnormal production of 18-oxocortisol and 18-hydroxycortisol.
This condition has no sub-types.