Wilson disease presents as a rare genetic condition that leads to the build-up of copper within various organs. This worsening condition often affect the liver, brain, eyes, and other organs. Symptoms vary widely can present as liver damage, neurological problems, and eye issues. Early detection and treatment are essential in mitigating the progres… 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