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Food supplements are not a substitute for a balanced and varied diet and a healthy lifestyle

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Primary carnitine deficiency is a rare autosomal recessive genetic disease affecting 1:40 000-1:120 000 individuals.2 It is caused by the presence of 2 mutated alleles (either in homozygosity or 2 mutations in compound heterozygosity) in SLC22A5, which codes for the OCTN2 transporter, responsible for intracellular carnitine transport

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The Phase II Detoxification Pathway Phase II is all about removing the freed-up toxic waste created in Phase I

At 12 weeks no muscle carnitine differences were apparent between the groups