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Wilson disease is a rare genetic illness that causes excessive storage of copper throughout various organs. This worsening condition may damage the liver, brain, eyes, and other systems. Symptoms range widely can present as nausea, vomiting, and tremors. Early identification and treatment play a vital role in preventing the advancement of this life
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Wilson's disease is a rare genetic disorder that causes a buildup of copper in the body. This can lead to critical damage to the liver, brain, and other organs. Symptoms often appear gradually and may include fatigue, jaundice, abdominal pain, tremors, and personality changes. Diagnosis typically involves blood tests to measure copper levels and g