Systematic review explores cardiac dysfunction mechanisms and management strategies in Wilson's disease, suggesting diagnostic advancements.
Introduction Wilson's disease (WD) is a rare autosomal recessive disorder caused by ATP7B gene mutations, leading to systemic copper accumulation. This systematic review examines the cardiac manifestations of WD and aims to summarize key diagnostic and therapeutic findings from available studies.
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Hullon et al. (2025) studied this question.
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