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Wilson disease affects the rare genetic disorder that causes the build-up of copper within certain organs. This worsening condition may damage the liver, brain, eyes, and other tissues. Symptoms vary widely can present as fatigue, jaundice, and abdominal pain. Early identification and treatment are essential in slowing down the advancement of this
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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 regulating 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