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Wilson disease affects the rare genetic illness that causes an accumulation of copper in certain organs. This deteriorating condition may damage the liver, brain, eyes, and other systems. Symptoms differ widely often manifest fatigue, jaundice, and abdominal pain. Early diagnosis and treatment play a vital role in mitigating the advancement of this
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Wilson disease is a rare genetic disorder characterized by the body's inability to properly discharge 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