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Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl

Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl: Introduction

Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl: An inherited organic acid disorder where an enzyme 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. The disorder results from a combined synthesis defect of AdoCbl and MeCbl. More detailed information about the symptoms, causes, and treatments of Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl is available below.

Symptoms of Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl

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Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl: Complications

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Causes of Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl

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Disease Topics Related To Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl

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Misdiagnosis and Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl

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More information about Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl

  1. Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
 

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