Marfan Syndrome Report

Marfan SyndromeMarfan syndrome is a genetic disorder that affects the connective tissue of the body and can cause a variety of symptoms, including skeletal abnormalities, cardiovascular complications, and vision problems. Marfan syndrome is caused by mutations in the fibrillin-1 (FBN1) gene, and this report tests for genetic variants that are known to affect this gene.More than 25 genes analyzed It is recommended if: This report is designed for individuals with a family history of Marfan syndrome or individuals with symptoms of the condition, such as a tall and slender build, scoliosis, and heart murmur. 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: Marfan Syndrome