Epidermolysis Bullosa Report

Epidermolysis BullosaEpidermolysis Bullosa report is used to identify genetic variants associated with epidermolysis bullosa (EB), a group of rare genetic disorders characterized by skin fragility and blistering. EB is caused by mutations in genes encoding proteins involved in maintaining the structure and integrity of the skin. This report tests for variants in these genes, which can help diagnose the specific subtype of EB and inform treatment and management decisions.More than 50 genes analyzed It is recommended if: This report is recommended for individuals with a family history of EB or individuals with symptoms such as blistering or skin erosions. Early diagnosis and proper management can improve quality of life and prevent complications such as infection and scarring. Genetic testing can also inform family planning decisions and provide reassurance for unaffected family members. List of main conditions: Epidermolysis Bullosa