There are 3 types of pseudohypoaldosteronism:
Inheritance is autosomal recessive or autosomal dominant.
Pseudohypoaldosteronism type I resembles other forms of hypoaldosteronism except that aldosterone levels are high.
The very rare pseudohypoaldosteronism type II is not discussed here.
The autosomal recessive form tends to be severe and permanent. Infants are resistant to the effects of aldosterone due to mutations causing decreased activity of the epithelial sodium channels (ENaC) located on the luminal membrane of the collecting tubule (overactivity of ENaC causes potassium excretion and sodium retention—see Liddle Syndrome Liddle Syndrome Liddle syndrome is a rare hereditary disorder involving increased activity of the epithelial sodium channel (ENaC), which causes the kidneys to excrete potassium but retain too much sodium and... read more ). The sodium channel in tissues other than the kidneys may be affected, leading to a miliary rash and/or complications similar to those of cystic fibrosis Cystic Fibrosis Cystic fibrosis is an inherited disease of the exocrine glands affecting primarily the gastrointestinal and respiratory systems. It leads to chronic lung disease, exocrine pancreatic insufficiency... read more .
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