Finally Find an Answer for You and Your Family
When you get a clear answer about Lynch syndrome, you can get a head start on prevention strategies and ahead of early signs of cancer.
Find your next step today.
Lynch syndrome, caused by an inherited mismatch repair (MMR) deficiency, is a genetic condition that increases the risk of developing certain types of cancer, primarily colorectal cancer and endometrial cancer.
Know your & your family’s risk
Lynch syndrome is inherited with 50% probability1 within affected families. Here’s what you need to know.When should I get tested?
If someone in your family has tested positive for Lynch syndrome or your healthcare provider has identified you at high risk of having Lynch syndrome, you should get tested.
Please consult with your doctor if you have concerns.
How do I get tested?
Traditional Lynch syndrome testing includes microsatellite instability tumor testing and DNA sequencing. Lynsight’s test, DiagMMR, is a new approach that provides exceptionally high fidelity results.
I’m positive for Lynch syndrome. now what?
A Lynch syndrome diagnosis puts you and your family on a proven path of screenings and beneficial lifestyle changes. Here are two important next steps.
Talk to your
healthcare provider
Schedule an appointment with your healthcare provider to discuss your diagnosis, explore personalized screening strategies, and develop a comprehensive care plan tailored to your needs.
Talk to
your family
Open and honest communication with your relatives about your diagnosis can empower them to make informed decisions about their own health. Together, you can take proactive steps to protect your family’s health for generations to come.
