Alport Syndrome Report

Alport SyndromeAlport Syndrome report is used to identify genetic variants associated with Alport syndrome, a rare inherited disorder that affects the kidneys and can lead to hearing loss and vision problems. This report tests for genetic variants in genes that encode collagen, a protein that is important for the structure and function of the kidneys, inner ear, and eyes.More than 8 genes analyzed It is recommended if: This report is designed for individuals with a family history of Alport syndrome or for those who have symptoms of the condition, such as blood in the urine, proteinuria, hearing loss, and vision problems. Early diagnosis through genetic testing can help inform treatment and management decisions, including kidney function monitoring, hearing and vision assessments, and supportive care. It can also inform family planning decisions and provide reassurance for unaffected family members. List of main conditions: Alport Syndrome