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Wilson disease affects the rare genetic disorder that leads to excessive storage of copper within certain organs. This deteriorating condition often impact the liver, brain, eyes, and other systems. Symptoms vary widely can present as fatigue, jaundice, and abdominal pain. Early identification and treatment play a vital role in preventing the devel
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Wilson disease is a rare genetic disorder characterized by the system's inability to properly eliminate excess copper. Normally, the liver plays a crucial role in managing copper levels, moving 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 thi