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As a result, your body will rely on its glucose reserves as an energy source

L-carnitine is a naturally occurring amino acid derivative that plays a crucial role in transporting long-chain fatty acids into the mitochondria, the energy centers of cells

There have been reported at least 15 syndromes in which carnitine deficiency seems to be secondary to genetic defects of intermediary metabolism or to other conditions [40]

The rate-limiting step in this process is the carnitine shuttle, specifically the CPT-I enzyme that attaches carnitine to long-chain fatty acids so they can cross the inner mitochondrial membrane

Although, the farther along the disease, the more drastic the treatment plan