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Wilson disease presents as a rare genetic condition that causes the build-up of copper within multiple organs. This progressive condition often impact the liver, brain, eyes, and other organs. Symptoms vary widely and plats faits maison may include nausea, vomiting, and tremors. Early identification and treatment are essential in mitigating the dev
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Wilson disease is a rare genetic disorder characterized by the body'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 t