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2-Methylbutyric Aciduria

2-Methylbutyric Aciduria: Introduction

2-Methylbutyric Aciduria: A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbutyryl-coenzyme A dehydrogenase) needed to convert the amino acid isoleucine into energy. 2-methylbutyrylglycine levels build up in the body and may cause damage. Symptoms vary according to the degree of enzyme deficiency - can range from asymptomatic to life-threatening. More detailed information about the symptoms, causes, and treatments of 2-Methylbutyric Aciduria is available below.

Symptoms of 2-Methylbutyric Aciduria

Home Diagnostic Testing

Home medical testing related to 2-Methylbutyric Aciduria:

Wrongly Diagnosed with 2-Methylbutyric Aciduria?

2-Methylbutyric Aciduria: Complications

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Causes of 2-Methylbutyric Aciduria

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2-Methylbutyric Aciduria: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and 2-Methylbutyric Aciduria

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2-Methylbutyric Aciduria: Research Doctors & Specialists

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2-Methylbutyric Aciduria: Broader Related Topics

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Related 2-Methylbutyric Aciduria Info

More information about 2-Methylbutyric Aciduria

  1. 2-Methylbutyric Aciduria: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
 

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