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[DOI] [PubMed] [Google Scholar] 34.Frye R.E., Rossignol D., Casanova M.F., Brown G.L., Martin V., Edelson S., Coben R., Lewine J., Slattery J.C., Lau C., et al

(Etiology) Carnitine-Acylcarnitine Translocase Deficiency Disorder is caused by mutations in the SLC25A20 gene, which provides instructions for making an enzyme called carnitine-acylcarnitine translocase (CACT), which is essential for fatty acid oxidation (a multistep process that breaks down (metabolizes) fats and converts them into energy) Fatty acid oxidation takes place within mitochondria

Gurlek, A., Tutar, E., Akcil, E., Dincer, I., Erol, C., Kocaturk, P

Medical history: Chronic hepatitis C (genotype 1A): Diagnosed in 28 years ago, likely acquired in 1985 after an automobile accident with multiple fractures and transfusion requirements

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