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Wilson disease affects the rare genetic disorder that leads to excessive storage of copper in multiple organs. This deteriorating condition can damage the liver, brain, eyes, and other tissues. Symptoms range widely can present as nausea, vomiting, and tremors. Early diagnosis and treatment play a vital role in slowing down the development of this

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