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The cerivastatin experience serves as a critical exemplar of the necessity for rigorous safety surveillance in statin pharmacotherapy and underscores the delicate equilibrium between therapeutic efficacy and the potential for serious, treatment-limiting toxicities

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Wilson disease is a disorder of copper metabolism, caused by biallelic mutations in the ATP7B gene, and characterized by low serum ceruloplasmin levels and elevated daily urinary copper excretion (Mulligan and Bronstein, 2020)