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Glutaricaciduria I

Glutaricaciduria I: Introduction

Glutaricaciduria I: A rare inherited enzyme deficiency disorder where deficiency of the glutaryl-CoA dehydrogenase enzyme results in dystonia, dyskinesia and sometimes mental retardation. More detailed information about the symptoms, causes, and treatments of Glutaricaciduria I is available below.

Symptoms of Glutaricaciduria I

Home Diagnostic Testing

Home medical testing related to Glutaricaciduria I:

Wrongly Diagnosed with Glutaricaciduria I?

Glutaricaciduria I: Deaths

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Glutaricaciduria I: Complications

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Causes of Glutaricaciduria I

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Disease Topics Related To Glutaricaciduria I

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Less Common Symptoms of Glutaricaciduria I

Glutaricaciduria I: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Glutaricaciduria I

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Glutaricaciduria I: Research Doctors & Specialists

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Statistics for Glutaricaciduria I

Glutaricaciduria I: Broader Related Topics

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Definitions of Glutaricaciduria I:

Glutaricaciduria I is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Glutaricaciduria I, or a subtype of Glutaricaciduria I, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Glutaricaciduria I

  1. Glutaricaciduria I: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Deaths
  8. Complications
 

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