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Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency

Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency: Introduction

Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency: An inherited organic acid disorder where an enzyme (Methylmalonyl CoA mutase apoenzyme) deficiency impairs the body's ability to break down certain proteins (methionine, threonine, isoleucine and valine) consumed in the diet. This results in a buildup of glycine and methylmalonic acid which results in harmful affects. More detailed information about the symptoms, causes, and treatments of Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency is available below.

Symptoms of Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency

Home Diagnostic Testing

Home medical testing related to Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency:

Wrongly Diagnosed with Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency?

Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency: Complications

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Causes of Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency

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Disease Topics Related To Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency

Research the causes of these diseases that are similar to, or related to, Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency:

Misdiagnosis and Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency

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Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency: Research Doctors & Specialists

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Related Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency Info

More information about Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency

  1. Methylmalonic acidemia, Methylmalonyl CoA mutase deficiency: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
 

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