Wilson Disease Report

Wilson DiseaseWilson disease is a rare inherited disorder that causes copper to accumulate in the body, leading to liver damage and neurological symptoms. Wilson disease is caused by mutations in a gene involved in copper transport and metabolism.1 or more genes analyzed It is recommended if: This report is designed for individuals with a family history of Wilson disease or individuals with symptoms of the condition, such as liver disease or neurological symptoms. Genetic testing can confirm a diagnosis, provide information on disease severity and progression, and inform treatment and management decisions. Testing can also inform family planning decisions and provide reassurance for unaffected family members. List of main conditions: Wilson disease