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Dysphagia in Wilson’s Disease: A Case Report of One-Year Follow-Up

Kim D, Park YG, Park JH, Park J

Wilson’s disease (WD) is a genetic disease caused by an ATP7B gene mutation. Although dysphagia is known as a neurological manifestation of WD, clinical case reports with post-treatment long-term follow-up...
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Late-Onset Wilson’s Disease Mimics Hashimoto Encephalopathy

Lee DY, Lee GH, Jung DS, Kim J

A 48-year-old woman presented with a 1-day history of aggressive behavior. Hashimoto encephalopathy was first suspected based on elevated levels of serum anti-thyroid peroxidase antibody. Her clinical symptoms did not...
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