Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer)

Lynch Syndrome, also known as Hereditary Nonpolyposis Colorectal Cancer (HNPCC), is a genetic condition that increases the risk of developing colorectal and other cancers. It occurs due to inherited mutations in genes responsible for fixing DNA errors, leading to a higher chance of cancer over time. People with Lynch Syndrome often develop cancer at a younger age and may have a family history of related cancers. Early detection through screening and regular medical check-ups can help manage the risk. It is important for individuals with a family history of these cancers to consult healthcare professionals for genetic testing and personalized care.