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What is Tyrosinemia, type III?

What is Tyrosinemia, type III?

  • 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.

Tyrosinemia, type III: Introduction

Types of Tyrosinemia, type III:

Broader types of Tyrosinemia, type III:

How many people get Tyrosinemia, type III?

Prevalance of Tyrosinemia, type III: only a few cases of tyrosinemia type III have been reported, Genetics Home Reference website

What causes Tyrosinemia, type III?

Causes of Tyrosinemia, type III: see causes of Tyrosinemia, type III

What are the symptoms of Tyrosinemia, type III?

Symptoms of Tyrosinemia, type III: see symptoms of Tyrosinemia, type III

Tyrosinemia, type III: Testing

Diagnostic testing: see tests for Tyrosinemia, type III.

Misdiagnosis: see misdiagnosis and Tyrosinemia, type III.

How is it treated?

Doctors and Medical Specialists for Tyrosinemia, type III: Medical Geneticist ; see also doctors and medical specialists for Tyrosinemia, type III.
Treatments for Tyrosinemia, type III: see treatments for Tyrosinemia, type III

Name and Aliases of Tyrosinemia, type III

Main name of condition: Tyrosinemia, type III

Other names or spellings for Tyrosinemia, type III:

Tyrosinemia III

Tyrosinemia, type III: Related Conditions

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

  • typeI tyrosinemia
  • Type II tyrosinemia
  • Type III tyrosinemia
  • Alkaptonuria
  • Onchronosis
  • Inborn errors of metabolism
 

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