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Methylmalonic acidemia, cobalamin A deficiency

Methylmalonic acidemia, cobalamin A deficiency: Introduction

Methylmalonic acidemia, cobalamin A deficiency: An inherited organic acid disorder where an enzyme deficiency (Cobalamin A 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, cobalamin A deficiency is available below.

Symptoms of Methylmalonic acidemia, cobalamin A deficiency

Wrongly Diagnosed with Methylmalonic acidemia, cobalamin A deficiency?

Methylmalonic acidemia, cobalamin A deficiency: Related Patient Stories

Methylmalonic acidemia, cobalamin A deficiency: Complications

Review possible medical complications related to Methylmalonic acidemia, cobalamin A deficiency:

Causes of Methylmalonic acidemia, cobalamin A deficiency

Read more about causes of Methylmalonic acidemia, cobalamin A deficiency.

Misdiagnosis and Methylmalonic acidemia, cobalamin A deficiency

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

Methylmalonic acidemia, cobalamin A deficiency: Broader Related Topics

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