Journal of pediatric endocrinology & metabolism : JPEM
Diagnostic pitfalls in aldosterone defects: a 9-year follow-up of early-onset pseudohypoaldosteronism type 2.
Mevra Cay, Ihsan Turan, Bahriye Atmıs, Leman Damla Kotan, Sukriye Tugce Celebi, Ayse Merve Cimen, Eda Mengen, Aysun Karabay Bayazıt, Bilgin Yuksel
Published: 202510.1515/jpem-2025-0526
Abstract
OBJECTIVES: Pseudohypoaldosteronism type 2 (PHA2) is a rare autosomal dominant electrolyte disorder characterized by hypertension, hyperkalemia, metabolic acidosis, and suppressed renin activity, usually with preserved renal function. Pathogenic vari…
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