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2,883 results

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Page 1
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. ...Some lesions (skull and mandible osteomas, dental abnormalities, and fibromas on …
Familial adenomatous polyposis (FAP) is characterized by the development of many tens to thousands of adenomas i …
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 …
CONTEXT.-: Familial adenomatous polyposis (FAP) is a rare genetic disorder with autosomal dominant inheritance, …
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. ...No consensus is reached on the right type and timing of colectomy. As patients w …
Familial adenomatous polyposis (FAP) and MUTYH-associated polyposis (MAP) are rare inherited polyposis …
Current management of familial adenomatous polyposis.
Lauricella S, Rausa E, Pellegrini I, Ricci MT, Signoroni S, Palassini E, Cavalcoli F, Pasanisi P, Colombo C, Vitellaro M. Lauricella S, et al. Expert Rev Anticancer Ther. 2024 Jun;24(6):363-377. doi: 10.1080/14737140.2024.2344649. Epub 2024 May 26. Expert Rev Anticancer Ther. 2024. PMID: 38785081 Review.
Individuals with APC-associated polyposis need to be managed by specialized multidisciplinary teams in dedicated centers. AREAS COVERED: The study aimed to review the literature on Familial adenomatous polyposis (FAP) to provide an update on dia …
Individuals with APC-associated polyposis need to be managed by specialized multidisciplinary teams in dedicated centers. AREAS COVER …
Guidelines for Familial Adenomatous Polyposis (FAP): challenges in defining clinical management for a rare disease.
Zare B, Monahan KJ. Zare B, et al. Fam Cancer. 2025 Apr 7;24(2):35. doi: 10.1007/s10689-025-00462-y. Fam Cancer. 2025. PMID: 40192835 Free PMC article. Review.
Recent updated management guidelines for Familial Adenomatous Polyposis (FAP) have been published by professional bodies internationally. ...The presence of a wide phenotypic spectrum in FAP and the other hereditary gastrointestinal polyposis …
Recent updated management guidelines for Familial Adenomatous Polyposis (FAP) have been published by professiona …
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 germlin …
Familial adenomatous polyposis (FAP) is a dominantly inherited familial cancer syndrome characterized by …
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. ...Several genotype-phenotype correlations ha …
Familial adenomatous polyposis (FAP) is an autosomal-dominant colorectal cancer syndrome, caused by a germline m …
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.
A multimodal approach of complementary techniques targeting primarily truncating, deletion and rearrangement mutations provides a robust screening protocol that identifies the vast majority of pathogenic germline APC gene mutations in FAP patients. Patients in whom no muta …
A multimodal approach of complementary techniques targeting primarily truncating, deletion and rearrangement mutations provides a robust scr …
The genetics of familial adenomatous polyposis (FAP) and MutYH-associated polyposis (MAP).
Claes K, Dahan K, Tejpar S, De Paepe A, Bonduelle M, Abramowicz M, Verellen C, Franchimont D, Van Cutsem E, Kartheuser A. Claes K, et al. Acta Gastroenterol Belg. 2011 Sep;74(3):421-6. Acta Gastroenterol Belg. 2011. PMID: 22103048 Free article. Review.
FAP is characterized by 100-1000s of adenomatous polyps in colon and rectum, and is in 70% of the patients associated with extracolonic manifestations. ...(A)FAP is caused by autosomal dominantly inherited mutations in the APC (Adenomatous polyposis …
FAP is characterized by 100-1000s of adenomatous polyps in colon and rectum, and is in 70% of the patients associated with ext …
[Familial adenomatous polyposis syndrome (FAP): pathogenesis and molecular mechanisms].
Friedrich A, Kullmann F. Friedrich A, et al. Med Klin (Munich). 2003 Dec 15;98(12):776-82. doi: 10.1007/s00063-003-1325-2. Med Klin (Munich). 2003. PMID: 14685680 Review. German.
The clinical and hereditary picture of the familial adenomatous polyposis syndrome (FAP) implied the existence of a single gene that regulates the formation of adenomatous polyps, the precursor for most colorectal cancers. The identification of …
The clinical and hereditary picture of the familial adenomatous polyposis syndrome (FAP) implied the existence o …
2,883 results