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By understanding the symptoms, causes, and management strategies, patients can navigate treatment effectively, improving their quality of life

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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)

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In scientific literature, DSIP is recognized as one of the first endogenous sleep-promoting substances identified, with potential roles in both sleep regulation and stress adaptation