Endocrinology Research and Practice
Original Article

Pseudohypoaldosteronism Type I: A Report of Two Cases

1.

Abant İzzet Baysal University, Düzce School of Medicine, Pediatrics, Düzce, Turkey

Endocrinol Res Pract 2001; 5: 43-45
Read: 1171 Downloads: 416 Published: 24 March 2022
ABSTRACT
Pseudohypoaldosteronism (PHA) i s characterised by salt wasting and failure to thrive in the newborn because of the resistance of mineralocorticoid receptors to aldosterone. The diagnosis is based on dehydration, hyponatremia, hyperkalemia, high urine sodium, and high serum concentrations of aldosterone and renin. The hyponatremia in PHA is not improved by exogenous mineralocorticoid administration without added sodium chloride. In this paper we reported two cases whose clinical and laboratory findings were compatible with the classical PHA. The hyponatremia of the cases was improved only by exogenous sodium chloride supplementation to their diets.
 
Files
EISSN 2822-6135