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Genetic Patient Navigation Fact Sheets/ Tool Kit Sheets #2

  • 1.  Genetic Patient Navigation Fact Sheets/ Tool Kit Sheets #2

    Posted 04-28-2020 14:29
    Dear Texas ONS Member,

    As part of the UT Southwestern's Cancer Prevention Research Institute of Texas' (CPRIT) grant, "The Dissemination of a Genetic Navigation Navigation Framework for Hereditary Cancers to Increase Mutation Carrier Identification and Improve Outcomes", I am attaching our Cancer Genetic Syndrome-Specific Fact Sheets and Clinician Guides for Lynch syndrome, the most common hereditary cancer syndrome, including a Spanish overview of Lynch syndrome.  The genes associated with Lynch syndrome are MLH1, MSH2, MSH6, PMS2 and EPCAM.  

    Our Cancer Genetics Toolkit is now online and available at Genetic Screening and Navigation Toolkit | Guide to Hereditary Cancer for Health Pros | UT Southwestern Medical Center.  Additional information/ tools will be updated over time. 

    Please do not hesitate to contact me with any questions or concerns.

    Thank you!

    Kathy

    ------------------------------
    Kathy Pratt, BSN, RN, OCN, CBCN, ONN-CG
    Genetic Patient Navigator
    Harold C. Simmons Comprehensive Cancer Center
    UT Southwestern Medical Center
    Dallas TX
    214-645-7302
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    Attachment(s)

    pdf
    EPCAM Clinical Guide.pdf   729 KB 1 version
    pdf
    EPCAM_Fact_Sheet.pdf   684 KB 1 version
    pdf
    MLH1 Clinical Guide.pdf   683 KB 1 version
    pdf
    MLH1_Fact_Sheet.pdf   667 KB 1 version
    pdf
    MSH2 Clinical Guide.pdf   680 KB 1 version
    pdf
    MSH2_Fact_Sheet.pdf   674 KB 1 version
    pdf
    MSH6 Clinical Guide.pdf   682 KB 1 version
    pdf
    MSH6_Fact_Sheet.pdf   667 KB 1 version
    pdf
    PMS2 Clinical Guide.pdf   672 KB 1 version
    pdf
    PMS2_Fact_Sheet.pdf   666 KB 1 version