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Wilson disease presents as a rare genetic illness that causes an accumulation of copper in certain organs. This progressive condition may affect the liver, brain, eyes, and other systems. Symptoms vary widely often manifest nausea, vomiting, and tremors. Early detection and treatment play a vital role in preventing the advancement of this debilitat
Wilson disease presents as a rare genetic illness that causes the build-up of copper throughout multiple organs. This worsening condition often affect the liver, brain, eyes, and other organs. Symptoms vary widely often manifest nausea, vomiting, and tremors. Early identification and treatment play a vital role in mitigating the advancement of this
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 processing 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 disrup