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Finally, a number of inherited mutations in genes involved in carnitine shuttling and fatty acid oxidation pathways do not systematically result in carnitine depletion (such that carnitine supplementation may not help mitigate the symptoms) but lead to abnormal profiles of acylcarnitine esters in blood (35, 40)

PMID: 31472821 3 A Rare Treatable Cause of Cardiomyopathy: Primary Carnitine Deficiency

Proper Disposal: Dispose of used needles and syringes in a puncture-resistant sharps container to prevent accidental needlestick injuries and contamination

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