Most people with wilson's disease are diagnosed between the ages of 5 and 35 But younger and older people can be affected too. Symptoms are typically related to the brain and liver Wilson disease is a genetic condition that causes copper to accumulate in your body Wilson disease, also known as hepatolenticular degeneration, is a rare autosomal recessive disorder caused by mutations in the atp7b gene, leading to abnormal copper accumulation in the liver, brain, cornea, and other organs. Wilson disease (also referred to as hepatolenticular degeneration) is a genetic disorder of copper metabolism with an autosomal recessive pattern of inheritance that leads to impaired function of the intracellular copper transporter atp7b.
Wilson disease is a rare genetic disorder that is passed from parents to children (inherited) It prevents your body from getting rid of extra copper in your system. How does a person get wilson's disease Learn everything about it here. Wilson disease is an inherited condition that causes the body to retain excess copper The liver of a person who has wilson disease does not release copper into bile as it should
Wilson's disease is a genetic disorder in which copper builds up in the body, mainly in the liver and brain If you need help in understanding what any of these terms are, please follow the hyperlinks to our glossary.
OPEN
