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Wilson disease is a rare genetic disorder that leads to an accumulation of copper within certain organs. This progressive condition often damage the liver, brain, eyes, and other systems. Symptoms differ widely and may include fatigue, jaundice, and abdominal pain. Early detection and treatment are crucial in mitigating the progression of this life
Wilson disease affects the rare genetic illness that results in the build-up of copper throughout various organs. This deteriorating condition can affect the liver, brain, eyes, and other organs. Symptoms range widely and may include liver damage, neurological problems, and eye issues. Early diagnosis and treatment play a vital role in slowing down
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, 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