Below you will find more information about Xanthinuria from Medigest. If you believe that you are suffering from any of the symptoms of Xanthinuria it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Xanthinuria and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Xanthinuria comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.


Xanthinuria otherwise known as the Xanthine oxydase deficiency , is a genetic disorder which causes deficiency of xanthine oxidase which is an enzyme that is needed for converting the xanthine to uric acid.


Diagnosis includes examination of family history and certain medical tests.


Currently, there is no treatment available for Xanthinuria . However, there are treatment and maintenance needed to keep a balance fluid in the body and avoiding high purine foods.

Symptoms and Signs

Symptoms includes unusually high concentrations of xanthine in the blood and urine which can lead to renal problems and a xanthine kidney stones (Hille R. (2006). "Structure and Function of Xanthine Oxidoreductase" European Journal of Inorganic Chemistry 2006 (10), 1905-2095).


Xanthinuria or the Xanthine oxydase deficiency is said to be an inherited deficiency.

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