Hereditary Xanthinuria Type II

Hereditary xanthinuria is an autosomal recessive genetic disorder that results in the presence of excessive amounts of xanthine in the urine. Xanthine is a metabolic by-product in the metabolic breakdown of nucleic acids to uric acid. This increases the risk for formation of xanthine bladder or kidney stones and can cause serious kidney disease.

Possible Test Results :

  • Clear
  • Carrier
  • Affected
  • Hereditary Clear
  • Hereditary Carrier
  • Hereditary Affected
More XDH-MOCOS Information (opens a new window)