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Wilson disease is a rare genetic condition that leads to excessive storage of copper within multiple organs. This deteriorating condition often affect the liver, brain, eyes, and other systems. Symptoms differ widely can present as fatigue, jaundice, and abdominal pain. Early detection and treatment are essential in slowing down the progression of
Wilson disease presents as a rare genetic illness that results in an accumulation of copper in various organs. This deteriorating condition may impact the liver, brain, eyes, and other systems. Symptoms differ widely often manifest nausea, vomiting, and tremors. Early diagnosis and treatment are crucial in slowing down the advancement of this life-
Wilson disease is a rare genetic disorder characterized by the body's inability to properly remove excess copper. Normally, the liver plays a crucial role in managing copper levels, transporting 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