Wilson disease presents as a rare genetic disorder that leads to excessive storage of copper throughout multiple organs. This worsening condition can impact the liver, brain, eyes, and other systems. Symptoms differ widely can present as nausea, vomiting, and tremors. Early diagnosis and treatment play a vital role in slowing down the development o… Read More

Wilson disease is a rare genetic disorder characterized by the organism's inability to properly discharge excess copper. Normally, the liver plays a crucial role in regulating 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 d… Read More