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Wilson disease presents as a rare genetic condition that causes the build-up of copper throughout various organs. This progressive condition can impact the liver, brain, cuisiner simplement eyes, and other organs. Symptoms vary widely can present as fatigue, jaundice, and abdominal pain. Early detection and treatment play a vital role in mitigating
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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, 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