Lynch Syndrome Follow-Up Survey |
You are receiving this email because you had previously met with a genetic counselor at UT Southwestern or an affiliated site (Moncrief Cancer Institute, Parkland Hospital, John Peter Smith Hospital, Texas Health Resources, or the Center for Cancer and Blood Disorders) and have Lynch Syndrome (caused by inherited mutations in the MLH1, MSH2, MSH6, PMS2, or EPCAM genes).
The purpose of this confidential medical follow-up survey is to measure if families are receiving appropriate care. This information is also used to improve our understanding of Lynch Syndrome.
The survey will take less than 5 minutes to complete.
If you need assistance completing this survey, please contact the Genetic Patient Navigator, Kathy Pratt, at kathy.pratt@utsw.edu or 214-645-7302.
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