Wilson disease affects the rare genetic disorder that causes an accumulation of copper in certain organs. This deteriorating condition often impact the liver, brain, eyes, and other tissues. Symptoms differ widely can present as liver damage, neurological problems, and eye issues. Early detection and treatment are crucial in mitigating the developm… Read More

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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… Read More