Introduction: Wilson's diseaseis a genetic disorder in one in 30,000 people. German pathologist Friedrich Theodor von Fredric initially identified this disease in 1854 and gave it the name Samuel Wilson Disease in honour of a British neurologist. Wilson's illness is an extremely uncommon inherited condition. The liver, brain, and othe important organs are overly Copper accumulated in this condition. Between the ages of five and 35, disease occurs. Children between the ages of 5 and 35 are typically diagnosed with Wilson's disease, and symptoms usually manifest. Young and older people can both be affected by the disease. Hepatolenticular Degeneration Syndrome and Copper Storage Disease are other names for this condition.

Wilson’sdisease, genetic disorder, excessive accumulation of Copper, health problems.