Fig. 2From: Novel SCNN1A gene splicing-site mutation causing autosomal recessive pseudohypoaldosteronism type 1 (PHA1) in two Italian patients belonging to the same small townFirst patient’s renal and urinary tract ultrasound: small hyperechoic formations, compatible with calcium oxalate crystals, in the left kidney (the arrow indicates the largest, with maximum diameter of about 3 mm) and bladder (the arrow indicates their sediment)Back to article page