2,4-dienyl-CoA reductase deficiency is a genetic condition and there is no cure. A person will never outgrow the disorder. One infant had a change in the NADK2 gene. 2,4-dienyl-CoA reductase deficiency is classified as a fatty acid oxidation disorder (FOD) and a mitochondrial disorder. Because so few people have had the disorder, doctors do not know the best way to treat it. Doctors also don’t know for sure what complications are associated with 2,4-dienyl-CoA reductase deficiency and making specific assessments about life expectancy are difficult.
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