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Xanthine oxidase deficiency type I

Xanthine oxidase deficiency type I: Introduction

Xanthine oxidase deficiency type I: A rare metabolic disorder characterized by excessive levels of xanthine in the urine. Type I xanthinuria is caused by a deficiency of the enzyme xanthine dehydrogenase which is needed to metabolize xanthine. The metabolic abnormality primarily causes kidney stones and kidney failure in severe cases. More detailed information about the symptoms, causes, and treatments of Xanthine oxidase deficiency type I is available below.

Symptoms of Xanthine oxidase deficiency type I

Wrongly Diagnosed with Xanthine oxidase deficiency type I?

Xanthine oxidase deficiency type I: Complications

Review possible medical complications related to Xanthine oxidase deficiency type I:

Causes of Xanthine oxidase deficiency type I

Read more about causes of Xanthine oxidase deficiency type I.

Disease Topics Related To Xanthine oxidase deficiency type I

Research the causes of these diseases that are similar to, or related to, Xanthine oxidase deficiency type I:

Misdiagnosis and Xanthine oxidase deficiency type I

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis). See ...read more »

Prognosis for Xanthine oxidase deficiency type I

Prognosis for Xanthine oxidase deficiency type I: varies from asymptomatic to renal failure

Xanthine oxidase deficiency type I: Broader Related Topics

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More information about Xanthine oxidase deficiency type I

  1. Xanthine oxidase deficiency type I: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Complications
  7. Prognosis
 

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