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Wilson disease is a rare genetic illness that leads to the build-up of copper throughout various organs. This deteriorating condition can damage the liver, brain, eyes, and other systems. Symptoms differ widely can present as liver damage, neurological problems, and eye issues. Early diagnosis and treatment play a vital role in mitigating the advan
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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 regulating 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 t