Renal tubular acidosis type 1 involves a pathology in the distal tubule that prevents it from excreting hydrogen ions, resulting in high urinary pH and low serum potassium.
Renal tubular acidosis type 2 involves a pathology in the proximal tubule that prevents it from reabsorbing bicarbonate, resulting in high urinary pH and high serum potassium.
Renal tubular acidosis type 4, the most common type, involves inadequate hydrogen excretion in the distal tubules, with both type 1 and 4 involving inadequate hydrogen excretion.
Type 2 Renal Tubular Acidosis (or proximal RTA) occurs when the proximal tubule cannot reabsorb bicarbonate from the urine to the blood, with excessive bicarbonate excreted in the urine.
Renal tubular acidosis presents with failure to thrive in children, recurrent UTIs, bone disease (rickets or osteomalacia), muscle weakness, arrhythmias, and hypokalaemia.