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How long does treatment take

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)

Sometimes tendons become irritated and inflamed or other swelling occurring in the hand or wrist narrows the size of the carpal tunnel in a way that pinches the median nerve