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Wilson disease presents as a rare genetic condition that causes the build-up of copper in various organs. This worsening condition can impact the liver, brain, eyes, and other organs. Symptoms differ widely can present as liver damage, neurological problems, and eye issues. Early diagnosis and treatment are crucial in mitigating the advancement of
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Wilson disease is a rare genetic disorder characterized by the body's inability to properly discharge excess copper. Normally, the liver plays a crucial role in managing copper levels, transporting 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