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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

Research the causes of these diseases that are similar to, or related to, Tyrosinemia, type III:

Misdiagnosis and Tyrosinemia, type III

Unnecessary hysterectomies due to undiagnosed bleeding disorder in women: The bleeding disorder called Von Willebrand's disease is quite common in women, more »

Tyrosinemia, type III: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Tyrosinemia, type III: Animations

Statistics for Tyrosinemia, type III

Tyrosinemia, type III: Broader Related Topics

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Related Tyrosinemia, type III Info

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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