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Studies show that GH deficiency is associated with increased slow-wave sleep (SWS) intensity, likely due to overactive hypothalamic GHRH

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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)