Adaptation and early implementation of the PREdiction model for gene mutations (PREMM5™) for lynch syndrome risk assessment in a diverse population

Adaptation and early implementation of the PREdiction model for gene mutations (PREMM5™) for lynch syndrome risk assessment in a diverse population

Lynch syndrome (LS) is the most common inherited cause of colorectal and endometrial cancers. Identifying individuals at risk for LS without personal cancer history requires detailed collection and assessment of family health history. However, barriers exist to family health history collection, espe...

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Bibliographic Details
Main Authors: Allen, J. (Author), Anderson, K.P (Author), Eubanks, D.J (Author), Feigelson, H.S (Author), Gilmore, M.J (Author), Goddard, K.A.B (Author), Hunter, J.E (Author), Kauffman, T.L (Author), Leo, M.C (Author), Lindberg, N.M (Author), McMullen, C. (Author), Mittendorf, K.F (Author), Sasaki, S.O (Author), Shuster, E. (Author), Syngal, S. (Author), Ukaegbu, C. (Author), Wilfond, B.S (Author), Zepp, J.M (Author)
Format: Article
Language:English
Published: Springer Science and Business Media B.V. 2022
Subjects:
Family history
Hereditary cancer
Lynch syndrome
Risk assessment
Underserved
Online Access:View Fulltext in Publisher

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