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There are a bunch of other inborn errors of metabolism, including short-chain acyl-CoA dehydrogenase deficiency and medium-chain acyl-CoA dehydrogenase deficiency.[ref] Lets look at the inborn errors of metabolism involving carnitine: CPT2 gene: The CPT2 gene encodes the enzyme that moves fatty acids attached to carnitine into the inner membrane of the mitochondria

Cancer 109 , 574580 (2007)

This may in part be because gut bacteria metabolise l-carnitine into a compound called trimethylamine-N-oxide (TMAO), which is known to cause furring of the arteries and potentially lead to atherosclerosis Thyroid function: taking l-carnitine as a supplement can make the symptoms of a low-functioning thyroid worse Muscle weakness and seizures: high amounts of l-carnitine may cause muscle weakness in those with chronic kidney disease and may increase the risk of seizures in those with seizure-related disorders Food sources of carnitine There are many natural food sources of carnitine

Triazine herbicides and their chlorometabolites alter steroidogenesis in BLTK1 murine Leydig cells

La L-carnitine suscite donc un intrt particulier, aussi bien dans le domaine mdical que nutritionnel, et son utilisation sous forme de complments alimentaires est de plus en plus frquente

PMCID: PMC3784205