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Wilson disease is a rare genetic illness that leads to an accumulation of copper in various organs. This deteriorating condition often damage the liver, brain, eyes, and other tissues. Symptoms range widely can present as liver damage, neurological problems, and eye issues. Early identification and treatment are crucial in preventing the progressio
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, 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