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[Familial colorectal cancer].
Ugeskr Laeger. 2006 Jun 12; 168(24):2369-73.UL

Abstract

The most frequent monogenic predisposition to CRC is hereditary non-polyposis colorectal cancer (HNPCC). Less frequent are syndromes with polyposis. In some families the occurrence of CRC indicates a familial risk of CRC without the diagnostic criteria for the above syndromes being fulfilled. In families where causative mutations are identified, predictive genetic testing is offered. When no mutation is identified in a family, the risk of individual members of the family is evaluated according to the family history. Individuals with a high risk of CRC are offered surveillance.

Authors+Show Affiliations

Arhus Universitetshospital, Arhus Sygehus, Klinisk Genetisk Afdeling, Onkogenetisk Klinik, DK-8000 Arhus C. lsund@as.aaa.dkNo affiliation info availableNo affiliation info available

Pub Type(s)

English Abstract
Journal Article

Language

dan

PubMed ID

16822423

Citation

Sunde, Lone E M., et al. "[Familial Colorectal Cancer]." Ugeskrift for Laeger, vol. 168, no. 24, 2006, pp. 2369-73.
Sunde LE, Bülow S, Bernstein IT. [Familial colorectal cancer]. Ugeskr Laeg. 2006;168(24):2369-73.
Sunde, L. E., Bülow, S., & Bernstein, I. T. (2006). [Familial colorectal cancer]. Ugeskrift for Laeger, 168(24), 2369-73.
Sunde LE, Bülow S, Bernstein IT. [Familial Colorectal Cancer]. Ugeskr Laeg. 2006 Jun 12;168(24):2369-73. PubMed PMID: 16822423.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Familial colorectal cancer]. AU - Sunde,Lone E M, AU - Bülow,Steffen, AU - Bernstein,Inge T, PY - 2006/7/11/pubmed PY - 2006/7/13/medline PY - 2006/7/11/entrez SP - 2369 EP - 73 JF - Ugeskrift for laeger JO - Ugeskr. Laeg. VL - 168 IS - 24 N2 - The most frequent monogenic predisposition to CRC is hereditary non-polyposis colorectal cancer (HNPCC). Less frequent are syndromes with polyposis. In some families the occurrence of CRC indicates a familial risk of CRC without the diagnostic criteria for the above syndromes being fulfilled. In families where causative mutations are identified, predictive genetic testing is offered. When no mutation is identified in a family, the risk of individual members of the family is evaluated according to the family history. Individuals with a high risk of CRC are offered surveillance. SN - 1603-6824 UR - https://www.unboundmedicine.com/medline/citation/16822423/[Familial_colorectal_cancer]_ L2 - http://www.diseaseinfosearch.org/result/2734 DB - PRIME DP - Unbound Medicine ER -