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1,570 results

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Page 1
Familial Adenomatous Polyposis Syndrome: An Update and Review of Extraintestinal Manifestations.
Dinarvand P, Davaro EP, Doan JV, Ising ME, Evans NR, Phillips NJ, Lai J, Guzman MA. Dinarvand P, et al. Arch Pathol Lab Med. 2019 Nov;143(11):1382-1398. doi: 10.5858/arpa.2018-0570-RA. Epub 2019 May 9. Arch Pathol Lab Med. 2019. PMID: 31070935 Free article. Review.
CONTEXT.-: Familial adenomatous polyposis (FAP) is a rare genetic disorder with autosomal dominant inheritance, defined by numerous adenomatous polyps, which inevitably progress to colorectal carcinoma unless detected and managed early. ...These manifestation …
CONTEXT.-: Familial adenomatous polyposis (FAP) is a rare genetic disorder with autosomal dominant inheritance, defined by num …
Management of familial adenomatous polyposis and MUTYH-associated polyposis; new insights.
Aelvoet AS, Buttitta F, Ricciardiello L, Dekker E. Aelvoet AS, et al. Best Pract Res Clin Gastroenterol. 2022 Jun-Aug;58-59:101793. doi: 10.1016/j.bpg.2022.101793. Epub 2022 Mar 16. Best Pract Res Clin Gastroenterol. 2022. PMID: 35988966 Free article. Review.
Familial adenomatous polyposis (FAP) and MUTYH-associated polyposis (MAP) are rare inherited polyposis syndromes with a high colorectal cancer (CRC) risk. ...Whereas up until recently upper gastrointestinal surveillance was mostly diagnostic and patien …
Familial adenomatous polyposis (FAP) and MUTYH-associated polyposis (MAP) are rare inherited polyposis syndromes …
Familial adenomatous polyposis.
Half E, Bercovich D, Rozen P. Half E, et al. Orphanet J Rare Dis. 2009 Oct 12;4:22. doi: 10.1186/1750-1172-4-22. Orphanet J Rare Dis. 2009. PMID: 19822006 Free PMC article. Review.
Familial adenomatous polyposis (FAP) is characterized by the development of many tens to thousands of adenomas in the rectum and colon during the second decade of life. ...Classic FAP is inherited in an autosomal dominant manner and results from a germline mutation …
Familial adenomatous polyposis (FAP) is characterized by the development of many tens to thousands of adenomas in the rectum a …
Familial and hereditary gastric cancer, an overview.
Carneiro F. Carneiro F. Best Pract Res Clin Gastroenterol. 2022 Jun-Aug;58-59:101800. doi: 10.1016/j.bpg.2022.101800. Epub 2022 May 4. Best Pract Res Clin Gastroenterol. 2022. PMID: 35988963 Review.
There are three major hereditable syndromes that affect primarily the stomach: hereditary diffuse gastric cancer (HDGC), gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS) and familial intestinal gastric cancer (FIGC). HDGC is caused by germline mutations …
There are three major hereditable syndromes that affect primarily the stomach: hereditary diffuse gastric cancer (HDGC), gastric adenocarcin …
Hereditary colorectal, gastric, and pancreatic cancer: comprehensive review.
Seppälä TT, Burkhart RA, Katona BW. Seppälä TT, et al. BJS Open. 2023 May 5;7(3):zrad023. doi: 10.1093/bjsopen/zrad023. BJS Open. 2023. PMID: 37165697 Free PMC article. Review.
RESULTS: Lynch syndrome, formerly known as hereditary non-polyposis colorectal cancer, increases the risk of several abdominal cancers, with the highest population prevalence. Familial adenomatous polyposis and some of the more infrequent polyposis syn …
RESULTS: Lynch syndrome, formerly known as hereditary non-polyposis colorectal cancer, increases the risk of several abdominal cancer …
Evolving strategies for management of desmoid tumor.
Riedel RF, Agulnik M. Riedel RF, et al. Cancer. 2022 Aug 15;128(16):3027-3040. doi: 10.1002/cncr.34332. Epub 2022 Jun 7. Cancer. 2022. PMID: 35670122 Free PMC article. Review.
Most DTs are sporadic, harboring somatic mutations in the gene that encodes for beta-catenin, whereas DTs occurring in patients with familial adenomatous polyposis have germline mutations in the APC gene, which encodes for a protein regulator of beta-catenin. ...
Most DTs are sporadic, harboring somatic mutations in the gene that encodes for beta-catenin, whereas DTs occurring in patients with familia …
Molecular genetics of colorectal cancer.
Fearon ER. Fearon ER. Annu Rev Pathol. 2011;6:479-507. doi: 10.1146/annurev-pathol-011110-130235. Annu Rev Pathol. 2011. PMID: 21090969 Review.
Familial adenomatous polyposis.
Lal G, Gallinger S. Lal G, et al. Semin Surg Oncol. 2000 Jun;18(4):314-23. doi: 10.1002/(sici)1098-2388(200006)18:4<314::aid-ssu6>3.0.co;2-9. Semin Surg Oncol. 2000. PMID: 10805953 Review.
Familial adenomatous polyposis (FAP) is a dominantly inherited familial cancer syndrome characterized by an increased predisposition to colorectal cancer and other benign and malignant extra-colonic lesions. FAP has been linked to germline mutations of the adenom …
Familial adenomatous polyposis (FAP) is a dominantly inherited familial cancer syndrome characterized by an increased predispo …
Familial adenomatous polyposis.
Macrae F, du Sart D, Nasioulas S. Macrae F, et al. Best Pract Res Clin Gastroenterol. 2009;23(2):197-207. doi: 10.1016/j.bpg.2009.02.010. Best Pract Res Clin Gastroenterol. 2009. PMID: 19414146 Free article. Review.
Patients in whom no mutation is identified through this mutation protocol, may be sub-cohorts representing a different FAP pathogenesis including MYH associated polyposis and somatic cell mosaicism for APC gene mutations....
Patients in whom no mutation is identified through this mutation protocol, may be sub-cohorts representing a different FAP pathogenesis incl …
Familial adenomatous polyposis.
Galiatsatos P, Foulkes WD. Galiatsatos P, et al. Am J Gastroenterol. 2006 Feb;101(2):385-98. doi: 10.1111/j.1572-0241.2006.00375.x. Am J Gastroenterol. 2006. PMID: 16454848 Review.
Familial adenomatous polyposis (FAP) is an autosomal-dominant colorectal cancer syndrome, caused by a germline mutation in the adenomatous polyposis coli (APC) gene, on chromosome 5q21. It is characterized by hundreds of adenomatous color …
Familial adenomatous polyposis (FAP) is an autosomal-dominant colorectal cancer syndrome, caused by a germline mutation in the …
1,570 results