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- W2099647590 endingPage "258" @default.
- W2099647590 startingPage "237" @default.
- W2099647590 abstract "Colorectal cancer due to hereditary syndromes comprises approximately 5% of the overall colorectal cancer burden. Conditions fall into two distinct categories, the polyposis syndromes and hereditary non-polyposis colorectal cancer. It is important for the clinician to have a working knowledge of both as screening and surveillance recommendations differ significantly from those applicable to the general population. The polyposis syndromes include familial adenomatous polyposis, Peutz-Jeghers syndrome, juvenile polyposis, and Cowden syndrome. For each condition, a review of both the intestinal and extra-intestinal clinical findings is presented as well as the genetic basis, genetic testing, screening, surveillance and treatment options. As genetic testing for several of these conditions has recently become both commercially available and standard practice, special attention is given to indications and strategies for genetic testing in hereditary colorectal cancer syndromes." @default.
- W2099647590 created "2016-06-24" @default.
- W2099647590 creator A5014535384 @default.
- W2099647590 creator A5056740974 @default.
- W2099647590 date "2003-04-01" @default.
- W2099647590 modified "2023-10-16" @default.
- W2099647590 title "Hereditary polyposis syndromes and hereditary non-polyposis colorectal cancer" @default.
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- W2099647590 doi "https://doi.org/10.1016/s1521-6918(02)00149-x" @default.
- W2099647590 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/12676117" @default.
- W2099647590 hasPublicationYear "2003" @default.