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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)
Avoid frequent lip licking and contact with allergens or irritating chemicals
When administered under professional supervision at Krisha Hospital, the treatment is safe and well-tolerated by most individuals
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