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Wilson disease affects the rare genetic disorder that leads to the build-up of copper throughout certain organs. This worsening condition can affect the liver, brain, eyes, and other systems. Symptoms range widely can present as liver damage, neurological problems, and eye issues. Early detection and treatment play a vital role in slowing down the

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Wilson disease is a rare genetic disorder characterized by the system's inability to properly remove excess copper. Normally, the liver plays a crucial role in managing 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 this