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Optimizing Hereditary Cancer Risk Assessment for Lynch Syndrome in Gastroenterology Practice

This resource explores strategies to enhance cancer risk assessment and testing for Lynch syndrome in gastroenterology. It discusses the prevalence of mutations and high cancer risks associated with Lynch syndrome, emphasizing the importance of family history assessment. A standardized approach to risk assessment is presented, alongside the PREMM1,2,6 clinical prediction model which estimates gene-specific risk. The document also reviews genetic testing results and survey findings from patients and providers, highlighting the clinical benefits of proactive screening for Lynch syndrome-related cancers.

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Optimizing Hereditary Cancer Risk Assessment for Lynch Syndrome in Gastroenterology Practice

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