Von Willebrand Report

Von WillebrandVon Willebrand is a bleeding disorder caused by a deficiency or dysfunction of von Willebrand factor, a protein involved in blood clotting. Von Willebrand disease is caused by mutations in the von Willebrand factor gene, and this report tests for genetic variants that are known to affect these processes.More than 5 genes analyzed It is recommended if: This report is designed for individuals with a family history of bleeding disorders or individuals with symptoms of the condition, such as easy bruising, nosebleeds, and heavy menstrual bleeding. 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: Von Willebrand