Other Names for this Disease
- Isovaleric acid CoA dehydrogenase deficiency
- Isovaleryl CoA carboxylase deficiency
- IVD deficiency
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Isovaleric acidemia is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition.
Last updated: 5/16/2014
- Isovaleric acidemia. Genetics Home Reference (GHR). 2007; http://www.ghr.nlm.nih.gov/condition/isovaleric-acidemia. Accessed 5/16/2014.