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Wilson disease is a rare genetic condition that causes the build-up of copper within various organs. This worsening condition can affect the liver, brain, eyes, and other tissues. Symptoms range widely and may include liver damage, neurological problems, and eye issues. Early diagnosis and treatment are essential in mitigating the development of th
Wilson disease presents as a rare genetic condition that causes the build-up of copper throughout various organs. This deteriorating condition often impact the liver, brain, eyes, and other systems. Symptoms vary widely often manifest fatigue, jaundice, and abdominal pain. Early detection and treatment are crucial in preventing the development of t
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, 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 thi