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Wilson disease presents as a rare genetic illness that results in the build-up of copper within various organs. This progressive condition often affect the liver, brain, eyes, and other tissues. Symptoms vary widely often manifest liver damage, neurological problems, and eye issues. Early identification and treatment play a vital role in slowing do

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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 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 this