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Wilson disease affects the rare genetic illness that leads to the build-up of copper within certain organs. This worsening condition can affect the liver, disease wilson brain, eyes, and other organs. Symptoms range widely and may include liver damage, neurological problems, and eye issues. Early identification and treatment play a vital role in mi
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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 processing copper levels, carrying 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