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Familial hyperaldosteronism type IV

ORPHA:642671· ICD-10 E26.0

Definition

A rare familial hyperaldosteronism characterized by elevated aldosterone levels and low plasma renin activity, early-onset hypertension, and hypokalemia. Developmental delay, learning disabilities, behavioral abnormalities, and attention deficit disorder are observed in some patients.

Prevalence
<1 / 1 000 000
Age of onset
Adult, Childhood