Increasing Lynch Syndrome Identification Through Establishment of a Hereditary Colorectal Cancer Registry

2013 ◽  
Vol 56 (3) ◽  
pp. 308-314 ◽  
Author(s):  
Duveen Sturgeon ◽  
Tonna McCutcheon ◽  
Timothy M. Geiger ◽  
Roberta L. Muldoon ◽  
Alan J. Herline ◽  
...  
2014 ◽  
Vol 12 (5S) ◽  
pp. 829-831 ◽  
Author(s):  
Heather Hampel

NCCN has developed new guidelines for the assessment of high-risk familial/genetic colorectal cancer, and has positioned these recommendations within the guidelines for detection, prevention, and risk reduction. The Panel recommends that all patients with colorectal cancer be screened for Lynch syndrome, which occurs in 1 of every 35 patients and is the most common form of hereditary colorectal cancer. Such screening could be universal so that all tumors are genetically tested, or screening could be restricted to patients under the age of 70 and those aged 70 and older who meet clinical criteria.


2010 ◽  
Vol 9 (4) ◽  
pp. 563-570 ◽  
Author(s):  
Felipe Carneiro da Silva ◽  
Ligia Petrolini de Oliveira ◽  
Érika Monteiro Santos ◽  
Wilson Toshihiko Nakagawa ◽  
Samuel Aguiar Junior ◽  
...  

2017 ◽  
Vol 28 (4) ◽  
pp. 553-560
Author(s):  
J Church ◽  
M O’Malley ◽  
L Laguardia ◽  
D Crowe ◽  
X Xhaja ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document