Wilson disease is a rare genetic condition that leads to the build-up of copper throughout multiple organs. This deteriorating condition may affect the liver, brain, eyes, and other systems. Symptoms range widely often manifest liver damage, neurological problems, and eye issues. Early detection and treatment are crucial in preventing the advanceme… Read More

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Wilson disease is a rare genetic disorder characterized by the organism'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 t… Read More