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Glutaricaciduria type 3

Glutaricaciduria type 3: Introduction

Glutaricaciduria type 3: A very rare inherited metabolic disorder involving a deficiency of the glutaryl-CoA oxidase enzyme. The disorder is severe with death occurring during infancy or soon after birth. More detailed information about the symptoms, causes, and treatments of Glutaricaciduria type 3 is available below.

Symptoms of Glutaricaciduria type 3

Home Diagnostic Testing

Home medical testing related to Glutaricaciduria type 3:

Wrongly Diagnosed with Glutaricaciduria type 3?

Causes of Glutaricaciduria type 3

Read more about causes of Glutaricaciduria type 3.

Glutaricaciduria type 3: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Glutaricaciduria type 3

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Glutaricaciduria type 3: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Prognosis for Glutaricaciduria type 3

Prognosis for Glutaricaciduria type 3: death usually occurs around the time of birth or during infancy

Statistics for Glutaricaciduria type 3

Glutaricaciduria type 3: Broader Related Topics

User Interactive Forums

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Definitions of Glutaricaciduria type 3:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Glutaricaciduria type 3 as a "rare disease".
Source - Orphanet

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Videos about Glutaricaciduria type 3

 

More information about Glutaricaciduria type 3

  1. Glutaricaciduria type 3: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Prognosis
 

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