Pendred Syndrome Report

Pendred SyndromePendred syndrome is a genetic disorder that affects the development and function of the inner ear and the thyroid gland. Pendred syndrome is caused by mutations in the SLC26A4 gene, and this report tests for genetic variants in this gene.3 genes analyzed It is recommended if: This report is designed for individuals with a family history of Pendred syndrome or individuals with symptoms of the condition, such as hearing loss, balance problems, and goiter. 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: Pendred Syndrome