Lynch Syndrome

Disease

Disease Profile

Lynch syndrome is an inherited condition caused by pathogenic variants in DNA mismatch repair genes, leading to markedly increased lifetime risks of colorectal and other cancers. It is often associated with early-onset cancer in affected families.

Category
hereditary cancer predisposition syndrome
Prevalence
An estimated 1 in 279 people in the United States has Lynch syndrome.

Related News

Related Clinical Trials

NCT ID Title Status Phase
NCT07600710

Periodontal Disease in Patients With Lynch Syndrome

NOT_YET_RECRUITING
NCT07542405

A Web-Based Program (Kindred) to Improve the Understanding of Genetic Cancer Risk and Cancer Genetic Testing in African American Families

NOT_YET_RECRUITING NA
NCT07472686

Small Bowel Capsule Endoscopy in Lynch Syndrome

RECRUITING
NCT07450612

Liquid Biopsy and Machine Learning for Early Colorectal Cancer, Adenomas, Lynch Cancers, and Residual Disease Detection

RECRUITING
NCT07445828

Evaluation of Capsule Colonoscopy in Patients With Lynch Syndrome

NOT_YET_RECRUITING
NCT07436312

Impact of Consumption of Ultra-processed Foods in Individuals at High Risk of Cancer

RECRUITING NA
NCT07412197

Preventive Dendritic Cell Vaccination for Lynch Syndrome

NOT_YET_RECRUITING PHASE1/PHASE2
NCT07381985

Strategy for Management of Patients With Hereditary Cancer Syndromes (HCS) in a Rural Environment

ENROLLING_BY_INVITATION NA
NCT07360834

Study Aiming to Test Whether Non-invasive Liquid Biopsies Can Safely Reduce Invasive Surveillance Methods in Lynch Syndrome

NOT_YET_RECRUITING NA
NCT07304063

Overcoming Barriers to Uptake of Cascade Screening

NOT_YET_RECRUITING NA