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Wilson disease affects the rare genetic disorder that causes excessive storage of copper within certain organs. This deteriorating condition often impact the liver, brain, eyes, and other systems. Symptoms vary widely often manifest fatigue, jaundice, and abdominal pain. Early diagnosis and treatment are essential in slowing down the advancement of

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