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Furthermore, the study did not match variables because of the small populationpatients were not matched by their A1C or blood pressure, which are two important risk factors for developing NAION

Primary systemic carnitine deficiency Primary systemic carnitine deficiency is a rare, autosomal recessive disorder caused by mutations (including deletions) in the SLC22A5 gene coding for carnitine transporter protein OCTN2 (organic cation transporter novel 2) (33)

It mimics the physiological process and is subjected to feedback mechanisms, thus preventing adverse effects like improper dosing and disruption of normal processes