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Hereditary causes include genetic defects in the metabolism of amino acids, cholesterol, and fatty acids, such as propionyl-CoA carboxylase deficiency (aka propionic acidemia) and medium chain acyl-CoA dehydrogenase deficiency (36)

But some nutrients, like L-Carnitine, may be unfamiliar or completely foreign

Use of guidelines improves the neurological outcome in glutaric aciduria type I

Renal OCTN2 expression and activity increase when the carnitine concentration is reduced in the plasma and/or glomerular filtrate, whereas OCTN2 mRNA expression levels remain unchanged in the gut, liver, or skeletal muscle [254], highlighting the central role of the kidney in maintaining carnitine homeostasis

L-Carnitin dient dem Transport von Fettsuren aus dem Zellinneren in die Energiekraftwerke der Zelle, die Mitochondrien, wo die Fettverbrennung (Energiegewinnung) stattfindet