Wilson's disease is a rare genetic disorder that causes a buildup of copper in the body. This can lead to serious damage to the liver, brain, and other organs. Symptoms often develop gradually and may include fatigue, jaundice, abdominal pain, tremors, and personality changes. Diagnosis typically involves blood tests to measure copper levels and g
Wilson Disease: Unraveling the Genetics of Copper Poisoning
Wilson disease is a/presents as/manifests as a rare genetic disorder/illness/condition characterized by an inability to properly regulate/effectively manage/efficiently control copper levels/concentrations/storage. This condition results from/stems from/arises due to mutations in the ATP7B gene, which is responsible for/plays a vital role in/contro