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Wilson disease presents as a rare genetic illness that results in excessive storage of copper in certain organs. This worsening condition can impact the liver, brain, eyes, and other tissues. Symptoms differ widely can present as nausea, vomiting, and tremors. Early detection and treatment play a vital role in slowing down the advancement of this d
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Wilson disease is a rare genetic disorder characterized by the wilson disease copper metabolism system's inability to properly discharge excess copper. Normally, the liver plays a crucial role in processing copper levels, moving it to other parts of the body where it is needed for various functions. However, in individuals with Wilson disease, muta