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Molybdenum, cofactor deficiency, inherited

Molybdenum, cofactor deficiency, inherited: Introduction

Molybdenum, cofactor deficiency, inherited: A rare metabolic disorder characterized by excessive levels of xanthine in the urine. It is caused by a deficiency of the enzymes xanthine dehydrogenase (as in xanthinuria type I) and enzyme aldehyde oxidase (as in xanthinuria type II) as well as sulfite oxidase which are needed to metabolize xanthine. The metabolic abnormality causes severe xanthinuria with neurological symptoms. The condition may be an inherited or acquired (due to certain drug therapies) deficiency. More detailed information about the symptoms, causes, and treatments of Molybdenum, cofactor deficiency, inherited is available below.

Symptoms of Molybdenum, cofactor deficiency, inherited

Home Diagnostic Testing

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Molybdenum, cofactor deficiency, inherited: Complications

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Causes of Molybdenum, cofactor deficiency, inherited

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Disease Topics Related To Molybdenum, cofactor deficiency, inherited

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Molybdenum, cofactor deficiency, inherited: Undiagnosed Conditions

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Misdiagnosis and Molybdenum, cofactor deficiency, inherited

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Molybdenum, cofactor deficiency, inherited: Research Doctors & Specialists

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Prognosis for Molybdenum, cofactor deficiency, inherited

Prognosis for Molybdenum, cofactor deficiency, inherited: poor in congenital cases

Molybdenum, cofactor deficiency, inherited: Broader Related Topics

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More information about Molybdenum, cofactor deficiency, inherited

  1. Molybdenum, cofactor deficiency, inherited: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
  8. Prognosis
 

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