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Worldwide Practice Patterns in Lynch Syndrome Diagnosis and Management, Based on Data From the International Mismatch Repair Consortium Jennifer Y. Pan, Robert W. Haile, Allyson Templeton, Finlay Macrae, FeiFei Qin, Vandana Sundaram, Uri Ladabaum Clinical Gastroenterology and Hepatology Volume 16, Issue 12, Pages e11 (December 2018) DOI: /j.cgh Copyright © 2018 AGA Institute Terms and Conditions
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Figure 1 Estimated annual referrals and diagnoses for Lynch syndrome. Fifty-five percent of respondents provided estimates, and not rigorous ascertainment of results, which may affect the reliability of the numbers shown. Clinical Gastroenterology and Hepatology , e11DOI: ( /j.cgh ) Copyright © 2018 AGA Institute Terms and Conditions
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Figure 2 Programs for identifying new cases of Lynch syndrome. The percentage totals may not add up to 100% because of rounding and were based off a total of N = 54 as 1 respondent left the question unanswered. Clinical Gastroenterology and Hepatology , e11DOI: ( /j.cgh ) Copyright © 2018 AGA Institute Terms and Conditions
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Figure 3 Estimated uptake of genetic testing in at-risk family members. Fifty-five percent of respondents provided estimates, and not rigorous ascertainment of results, which may affect the reliability of the numbers shown. The percentage totals may not add up to 100% because of rounding and were based off a total of N = 54 because 1 respondent left the question unanswered. Clinical Gastroenterology and Hepatology , e11DOI: ( /j.cgh ) Copyright © 2018 AGA Institute Terms and Conditions
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Supplementary Figure 1 Germline testing approaches. (A) Use of multigene germline panels. (B) Testing for biallelic mutations in tumors. Clinical Gastroenterology and Hepatology , e11DOI: ( /j.cgh ) Copyright © 2018 AGA Institute Terms and Conditions
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