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Tyrosinemia, type III

Tyrosinemia, type III: Introduction

Tyrosinemia, type III: A very rare genetic metabolic disorder characterized by a deficiency of particular enzymes which prevents the breakdown of tyrosine which then builds up in the liver. Type III involves a deficiency of the enzyme 4-hydroxyphenlypyruvate dioxygenase. More detailed information about the symptoms, causes, and treatments of Tyrosinemia, type III is available below.

Symptoms of Tyrosinemia, type III

Home Diagnostic Testing

Home medical testing related to Tyrosinemia, type III:

Wrongly Diagnosed with Tyrosinemia, type III?

Causes of Tyrosinemia, type III

Read more about causes of Tyrosinemia, type III.

Disease Topics Related To Tyrosinemia, type III

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Misdiagnosis and Tyrosinemia, type III

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Tyrosinemia, type III: Research Doctors & Specialists

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Tyrosinemia, type III: Animations

Statistics for Tyrosinemia, type III

Tyrosinemia, type III: Broader Related Topics

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More information about Tyrosinemia, type III

  1. Tyrosinemia, type III: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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