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Foulkes, Karlsruhe Institute of Technology, Germany Received: August 13, 2012

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Primary carnitine deficiency (PCD) is an autosomal recessive disorder characterized by a lack of plasma membrane carnitine transport owing to a shortcoming in the OCTN2 carnitine transporter

However, most patients do not exhibit specific symptoms in the early stages of OC and CA125 has limited sensitivity and specificity for early cancer detection (Liu et al., 2020)