Methylmalonic acidemia

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List of terms related to Methylmalonic acidemia

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

Methylmalonic acidemia
Methylmalonic acid
ICD-10	E71.1
ICD-9	270.3
DiseasesDB	29509 Template:DiseasesDB2
MedlinePlus	001162
eMedicine	neuro/576

Overview

Methylmalonic acidemia (MMA, also known as "methylmalonic aciduria") is an inborn error of intermediary metabolism that may present in the early neonatal period with progressive encephalopathy and death due to a secondary hyperammonemia.

Methylmalonic acidemia does not always result in death, if it is diagnosed at an early age.

Classification

Types

• Online Mendelian Inheritance in Man (OMIM) 251100 - cblA type
• Online Mendelian Inheritance in Man (OMIM) 251110 - cblB type
• Online Mendelian Inheritance in Man (OMIM) 277400 - cblC type
• Online Mendelian Inheritance in Man (OMIM) 277410 - cblD type
• Online Mendelian Inheritance in Man (OMIM) 277380 - cblF type
• Online Mendelian Inheritance in Man (OMIM) 606169 - cblH type
• Online Mendelian Inheritance in Man (OMIM) 251000 - mut type

Cobalmin (vitamin B12) is also needed for the conversion of methylmalonyl-CoA to Succinyl-CoA. Mutations leading to defects in cobalmin or in its transport frequently result in the development of acidemia. The numerous pat

Causes

Methylmalonic acidemia is an inherited disorder in which the body is unable to process certain proteins and fats (lipids) properly. Methylmalonic acidemia is a disorder of amino acid metabolism, involving a defect in the conversion of methylmalonyl-coenzyme A (CoA) to succinyl-CoA by methylmalonyl-CoA mutase.

See also

• Isovaleric acidemia
• Propionic acidemia
• Methylmalonic acid

References

• Organic Acidemia Association
• Methylmalonic acidemia at NLM Genetics Home Reference
• Washington Health Center

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