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Introduction Wilsons disease is a genetic disorder characterised by abnormal copper metabolism, leading to excessive copper deposition , primarily in the liver and brain. The condition typically has a juvenile onset (before 16 years of age), though it can present at any stage of life

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Fischer GM, Yennu-Nanda VG, Tetzlaff MT, Lazar AJ, Carapeto F, de Macedo MP, Hudgens C, Holmen SL, Kircher DA, Knighton B, Davies MA

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Efficacy and safety of cagrilintide 2.4 mg in adults with overweight/obesity: data from REDEFINE 1