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Wilson disease affects the rare genetic illness that results in an accumulation of copper throughout certain organs. This deteriorating condition often damage the liver, brain, eyes, and other tissues. Symptoms differ widely and may include fatigue, jaundice, and abdominal pain. Early detection and treatment play a vital role in preventing the adva
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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 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 t