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Wilson disease is a rare genetic illness that causes an accumulation of copper within certain organs. This deteriorating condition may impact the liver, brain, eyes, and other tissues. Symptoms vary widely often manifest fatigue, jaundice, and abdominal pain. Early detection recettes and treatment play a vital role in preventing the development of
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Wilson disease is a rare genetic disorder characterized by the organism's inability to properly discharge excess copper. Normally, the liver plays a crucial role in processing copper levels, transporting it to other parts of the body where it is needed person with wilson disease for various functions. However, in individuals with Wilson disease, mu