Wilson disease affects the rare genetic illness that results in the build-up of copper within multiple organs. This worsening condition can damage the liver, brain, eyes, and other systems. Symptoms vary widely often manifest fatigue, jaundice, and abdominal pain. Early detection and treatment play a vital role in slowing down the development of th… Read More

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Wilson disease is a rare genetic disorder characterized by the system's inability to properly eliminate excess copper. Normally, the liver plays a crucial role in managing 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… Read More