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2-methylbutyryl-coenzyme A dehydrogenase deficiency

2-methylbutyryl-coenzyme A dehydrogenase deficiency: Introduction

2-methylbutyryl-coenzyme A dehydrogenase deficiency: 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-methylbutyryl-coenzyme A dehydrogenase deficiency is available below.

Symptoms of 2-methylbutyryl-coenzyme A dehydrogenase deficiency

Wrongly Diagnosed with 2-methylbutyryl-coenzyme A dehydrogenase deficiency?

2-methylbutyryl-coenzyme A dehydrogenase deficiency: Complications

Review possible medical complications related to 2-methylbutyryl-coenzyme A dehydrogenase deficiency:

Causes of 2-methylbutyryl-coenzyme A dehydrogenase deficiency

Read more about causes of 2-methylbutyryl-coenzyme A dehydrogenase deficiency.

Misdiagnosis and 2-methylbutyryl-coenzyme A dehydrogenase deficiency

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis...read more »

Statistics for 2-methylbutyryl-coenzyme A dehydrogenase deficiency

2-methylbutyryl-coenzyme A dehydrogenase deficiency: Broader Related Topics

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More information about 2-methylbutyryl-coenzyme A dehydrogenase deficiency

  1. 2-methylbutyryl-coenzyme A dehydrogenase deficiency: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Complications
 

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