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Carnitine transporter mutations in Crohn's disease consists of missense mutation(s) in the gene coding plasma membrane transporter OCTN1 (SLC22A4) and/or mutation(s) in the promoter of the gene encoding OCTN2 (SLC22A5) [14, 35]

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In general, the superficial lesions can be cured by surgical excision of the mole and adjacent tissues

Common sites: lower abdomen (2 inches from the navel), upper thigh, or proximal to the target injury

Future studies should aim to bridge this gap by providing direct evidence through well-designed clinical trials

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