3-methylcrotonyl-CoA carboxylase 2 deficiency

3-methylcrotonyl-CoA carboxylase 2 deficiency is a rare condition caused by a mutation in the MCCC2 gene. This condition is part of a group of metabolic disorders that affect how the body processes certain substances. It is defined as any 3-methylcrotonyl-CoA carboxylase deficiency where the cause is a mutation in the MCCC2 gene, making it distinct from other forms of the disorder.

Information about symptoms is currently limited for this condition.

This condition is caused by a genetic mutation in the MCCC2 gene. The mutation affects the proper function of the enzyme 3-methylcrotonyl-CoA carboxylase, which plays a role in the body’s metabolism.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about current research and future directions is currently limited for this condition.