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Hereditary Cancer Screening
Lynch Syndrome Panel
$599
This test identifies inherited mutations in genes associated with Lynch syndrome, the most common cause of hereditary colorectal cancer. It also increases risk for endometrial, ovarian, and other cancers.
Early Detection and Prevention
A diagnosis of Lynch syndrome allows for increased surveillance and preventative measures, which can significantly reduce the risk of developing cancer or detect it at an earlier, more treatable stage.
- Increased Surveillance: Qualify for more frequent colonoscopies and other screenings at an earlier age.
- Risk-Reducing Options: Discuss potential risk-reducing surgeries or medications with your doctor.
- Inform Your Family: Help close relatives understand their own potential risk and the importance of testing.
Who Should Consider This Test?
This test is recommended for individuals with a personal or family history of colorectal or endometrial cancer, especially if diagnosed under age 50, or those with multiple family members with Lynch-associated cancers.
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