TY - JOUR T1 - Unique eyelid manifestations in type 1 pseudohypoaldosteronism JF - Archives of Disease in Childhood - Fetal and Neonatal Edition JO - Arch Dis Child Fetal Neonatal Ed SP - F462 LP - F462 DO - 10.1136/archdischild-2011-301339 VL - 97 IS - 6 AU - Arwa Nasir AU - Issam Abou Najab Y1 - 2012/11/01 UR - http://fn.bmj.com/content/97/6/F462.abstract N2 - 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. … ER -