These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: Clinical genetics of hereditary colorectal cancer.
    Author: Power DG, Gloglowski E, Lipkin SM.
    Journal: Hematol Oncol Clin North Am; 2010 Oct; 24(5):837-59. PubMed ID: 20816577.
    Abstract:
    Colorectal cancer (CRC) is a common disease, and approximately 25% of patients have a familial component. High-penetrance singlegene germline mutations conferring a true hereditary susceptibility account for around 5% to 6% of all cases. Lynch syndrome is the most common hereditary form of colorectal cancer. Much of the hereditary component in the remaining familial cases of CRC is likely polygenic, and many of the genetic changes involved are as yet unidentified. This article addresses the most clinically important CRC genetic syndromes.
    [Abstract] [Full Text] [Related] [New Search]