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Wilson disease presents as a rare genetic illness that results in an accumulation of copper in multiple organs. This worsening condition can damage the liver, brain, eyes, and other tissues. Symptoms range widely often manifest nausea, vomiting, and tremors. Early identification and treatment play a vital role in slowing down the progression of thi
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Wilson disease is a rare genetic disorder characterized by the organism's inability to properly remove 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