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Wilson disease is a rare genetic illness that causes an accumulation of copper in multiple organs. This deteriorating condition often affect the liver, brain, eyes, and other tissues. Symptoms vary widely often manifest nausea, vomiting, and tremors. Early diagnosis and treatment are essential in preventing the progression of this debilitating dise
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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 managing 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 thi