Methylmalonic acidemia,
Introduction
- Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl: Introduction
- Summary Overview: Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl
Symptoms
- Symptoms of Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl
- Complications of Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl
Diagnosis
Misdiagnosis
- Misdiagnosis of Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl
- Undiagnosed Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl
Causes
- Causes of Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl
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Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl

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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Misdiagnosis and Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl

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