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Wilson disease is a rare genetic condition that causes excessive storage of copper in multiple organs. This deteriorating condition may impact the liver, brain, eyes, and other organs. Symptoms vary widely often manifest fatigue, jaundice, and abdominal pain. Early detection and treatment are crucial in slowing down the advancement of this serious
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Wilson disease is a rare genetic disorder characterized by the system's inability to properly remove excess copper. Normally, the liver plays a crucial role in regulating 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 th