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Familial pseudohypoaldosteronism type 1 (PHA1) occurs in two genetically and clinically distinguishable variants. Autosomal-recessive PHA1 that involves a genetic defect in the epithelial sodium channel that affects all aldosterone target organs including the kidney, colon and sweat glands.1 ,2 Two published case reports describe Meibomian gland involvement. …
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