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Wilson disease presents as a rare genetic disorder that leads to the build-up of copper within certain organs. This worsening condition may affect the liver, brain, eyes, and other tissues. Symptoms vary widely can present as fatigue, jaundice, and abdominal pain. Early diagnosis and treatment are essential in mitigating the advancement of this lif
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Wilson disease is a rare genetic disorder characterized by the system's inability to properly remove excess copper. Normally, the liver plays a crucial role in processing 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 this