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Harrisons Principles of Internal Medicine

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)

Sensors, 21(16), 5432

Laminoplasty Surgical reshaping or repositioning of the lamina to allow neural decompression

Unlike capsules or powders, sublingual peptides are designed to be placed under the tongue, where the thin mucosal tissue allows them to pass directly into the bloodstream

Advise patients to take oral quinolones at least 2 hours before or 4-6 hours after calcium supplements or calcium-fortified foods