Autosomal recessive distal renal tubular acidosis

The autosomal recessive form of distal renal tubular acidosis (dRTA) characterized by hypokalemic hyperchloremic metabolic acidosis. Deafness often occurs either early or later on in life but may be absent or never be diagnosed.

Also known as: AR dRTA, autosomal recessive distal RTA, autosomal recessive distal renal tubular acidosis (disease), distal renal tubular acidosis (disease), autosomal recessive

11 clinical trials for this condition and its sub-types.