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Primary carnitine deficiency (carnitine deficiency, systemic primary: CDSP) is an autosomal recessive disorder that results from the lack of function of the carnitine transporter, OCTN2

Thoughtfully developed with both ingredient quality and efficacy in mind, this innovative formula features topical Blue Copper Peptide (GHK-Cu) and Barley Seed Extract

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Patients with type 2 diabetes alongside obesity, where the strong glucose-lowering effect of tirzepatide is clinically useful

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The melanosomes in melanocytes residing in the basal cell layer of the epithelium can synthetise two chemically distinct types of melanin: brown/black eumelanin and red/yellow pheomelanin, both of which are derivatives of the amino acid tyrosine through the intermediate step of conversion of dopa to dopamine [4]