Wilson disease is a rare genetic condition that leads to the build-up of copper throughout multiple organs. This worsening condition may damage the liver, brain, eyes, and other tissues. Symptoms differ widely often manifest nausea, vomiting, and tremors. Early detection and idées de repas treatment play a vital role in mitigating the progression … Read More
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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, transporting 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 d… Read More