Wilson disease is a rare genetic condition that leads to excessive storage of copper throughout certain organs. This worsening condition may damage the liver, brain, eyes, and other tissues. Symptoms differ widely can present as liver damage, neurological problems, and eye issues. Early detection and treatment are essential in mitigating the wilson… Read More

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Wilson disease is a rare genetic disorder characterized by the system's inability to properly eliminate excess copper. Normally, the liver plays a crucial role in managing copper levels, moving it to other parts of the body where it is needed for various functions. However, in individuals with Wilson disease, mutations in the ATP7B gene disrupt thi… Read More