Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome)

Hereditary Nonpolyposis Colorectal Cancer, also known as Lynch Syndrome, is an inherited genetic condition that increases the risk of developing colorectal cancer and certain other cancers. It is caused by mutations in genes responsible for repairing DNA errors. People with Lynch Syndrome often develop cancer at a younger age and may have multiple relatives with related cancers. Early detection through regular screenings and genetic counseling can help manage and reduce risks. It’s important to know your family medical history and discuss it with a healthcare provider if Lynch Syndrome is suspected.