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Hamartomatous polyposis syndromes.
Calva D, Howe JR. Calva D, et al. Surg Clin North Am. 2008 Aug;88(4):779-817, vii. doi: 10.1016/j.suc.2008.05.002. Surg Clin North Am. 2008. PMID: 18672141 Free PMC article. Review.
These syndromes include juvenile polyposis, Peutz-Jeghers syndrome, hereditary mixed polyposis syndrome, and the phosphatase and tensin homolog gene (PTEN) hamartoma tumor syndromes (Cowden and Bannayan-Riley-Ruvalcaba syndromes), which are autosomal-d …
These syndromes include juvenile polyposis, Peutz-Jeghers syndrome, hereditary mixed polyposis syndrome, and the …
Hamartomatous polyposis syndrome associated malignancies: Risk, pathogenesis and endoscopic surveillance.
Liu S, Ma Y, You W, Li J, Li JN, Qian JM. Liu S, et al. J Dig Dis. 2021 Aug;22(8):444-451. doi: 10.1111/1751-2980.13029. Epub 2021 Jul 8. J Dig Dis. 2021. PMID: 34145757 Review.
Classical HPS includes juvenile polyposis syndrome, Peutz-Jeghers syndrome, PTEN hamartoma tumor syndrome and hereditary mixed polyposis syndrome. Patients with HPS have a higher risk of GI and extra-GI malignancies than the general population, althoug …
Classical HPS includes juvenile polyposis syndrome, Peutz-Jeghers syndrome, PTEN hamartoma tumor syndrome and hereditary mixed …
Hamartomatous polyposis syndromes: a review.
Jelsig AM, Qvist N, Brusgaard K, Nielsen CB, Hansen TP, Ousager LB. Jelsig AM, et al. Orphanet J Rare Dis. 2014 Jul 15;9:101. doi: 10.1186/1750-1172-9-101. Orphanet J Rare Dis. 2014. PMID: 25022750 Free PMC article. Review.
Hamartomatous Polyposis Syndromes (HPS) are genetic syndromes, which include Peutz-Jeghers syndrome, Juvenile polyposis syndrome, PTEN hamartoma tumour syndrome (Cowden Syndrom, Bannayan-Riley-Ruvalcaba and Proteus Syndrome) as well as hereditary mixed polyposis …
Hamartomatous Polyposis Syndromes (HPS) are genetic syndromes, which include Peutz-Jeghers syndrome, Juvenile polyposis syndrome, PTEN hamar …
Diagnosis and Management of Cancer Risk in the Gastrointestinal Hamartomatous Polyposis Syndromes: Recommendations From the US Multi-Society Task Force on Colorectal Cancer.
Boland CR, Idos GE, Durno C, Giardiello FM, Anderson JC, Burke CA, Dominitz JA, Gross S, Gupta S, Jacobson BC, Patel SG, Shaukat A, Syngal S, Robertson DJ. Boland CR, et al. Gastroenterology. 2022 Jun;162(7):2063-2085. doi: 10.1053/j.gastro.2022.02.021. Epub 2022 Apr 26. Gastroenterology. 2022. PMID: 35487791
They include Peutz-Jeghers syndrome, juvenile polyposis syndrome, the PTEN hamartoma tumor syndrome (including Cowden's syndrome and Bannayan-Riley-Ruvalcaba syndrome), and hereditary mixed polyposis syndrome. Diagnoses are based on clinical criteria a …
They include Peutz-Jeghers syndrome, juvenile polyposis syndrome, the PTEN hamartoma tumor syndrome (including Cowden's syndrome and Bannaya …
Genetics of the hamartomatous polyposis syndromes: a molecular review.
Chen HM, Fang JY. Chen HM, et al. Int J Colorectal Dis. 2009 Aug;24(8):865-74. doi: 10.1007/s00384-009-0714-2. Epub 2009 Apr 21. Int J Colorectal Dis. 2009. PMID: 19381654 Review.
MATERIALS AND METHODS: We searched for articles on inherited hamartomatous polyposis syndromes, including familial juvenile polyposis syndrome, Peutz-Jeghers syndrome, PTEN hamartoma tumor syndrome, multiple endocrine neoplasia syndrome 2B, hereditary mixed polyp …
MATERIALS AND METHODS: We searched for articles on inherited hamartomatous polyposis syndromes, including familial juvenile polyposis syndro …
Colorectal polyposes: from phenotype to diagnosis.
Jass JR. Jass JR. Pathol Res Pract. 2008;204(7):431-47. doi: 10.1016/j.prp.2008.03.008. Epub 2008 Jun 9. Pathol Res Pract. 2008. PMID: 18541388 Review.
The aim of this review is to highlight the principles and pitfalls in achieving a comprehensive description of the various types of colorectal polyposis, including classical FAP, attenuated FAP, MUTYH- (formerly MYH-) associated polyposis (MAP), other presentations of multiple ad …
The aim of this review is to highlight the principles and pitfalls in achieving a comprehensive description of the various types of colorect …
The hamartomatous polyposis syndromes: a clinical and molecular review.
Schreibman IR, Baker M, Amos C, McGarrity TJ. Schreibman IR, et al. Am J Gastroenterol. 2005 Feb;100(2):476-90. doi: 10.1111/j.1572-0241.2005.40237.x. Am J Gastroenterol. 2005. PMID: 15667510 Review.
Seven inherited hamartomatous polyposis syndromes have been described: familial juvenile polyposis syndrome, Cowden's syndrome, Bannayan-Ruvalcaba-Riley syndrome, Peutz-Jeghers syndrome, basal cell nevus syndrome, neurofibromatosis 1, and multiple endocrine neoplasia syndrome 2B. …
Seven inherited hamartomatous polyposis syndromes have been described: familial juvenile polyposis syndrome, Cowden's syndrome, Bannayan-Ruv …
Diagnosis and Management of Cancer Risk in the Gastrointestinal Hamartomatous Polyposis Syndromes: Recommendations From the US Multi-Society Task Force on Colorectal Cancer.
Boland CR, Idos GE, Durno C, Giardiello FM, Anderson JC, Burke CA, Dominitz JA, Gross S, Gupta S, Jacobson BC, Patel SG, Shaukat A, Syngal S, Robertson DJ. Boland CR, et al. Am J Gastroenterol. 2022 Jun 1;117(6):846-864. doi: 10.14309/ajg.0000000000001755. Epub 2022 Apr 26. Am J Gastroenterol. 2022. PMID: 35471415
They include Peutz-Jeghers syndrome, juvenile polyposis syndrome, the PTEN hamartoma tumor syndrome (including Cowden's syndrome and Bannayan-Riley-Ruvalcaba syndrome), and hereditary mixed polyposis syndrome. Diagnoses are based on clinical criteria a …
They include Peutz-Jeghers syndrome, juvenile polyposis syndrome, the PTEN hamartoma tumor syndrome (including Cowden's syndrome and Bannaya …
Diagnosis and management of cancer risk in the gastrointestinal hamartomatous polyposis syndromes: recommendations from the U.S. Multi-Society Task Force on Colorectal Cancer.
Boland CR, Idos GE, Durno C, Giardiello FM, Anderson JC, Burke CA, Dominitz JA, Gross S, Gupta S, Jacobson BC, Patel SG, Shaukat A, Syngal S, Robertson DJ. Boland CR, et al. Gastrointest Endosc. 2022 Jun;95(6):1025-1047. doi: 10.1016/j.gie.2022.02.044. Epub 2022 Apr 26. Gastrointest Endosc. 2022. PMID: 35487765
They include Peutz-Jeghers syndrome, juvenile polyposis syndrome, the PTEN hamartoma tumor syndrome (including Cowden's syndrome and Bannayan-Riley-Ruvalcaba syndrome), and hereditary mixed polyposis syndrome. Diagnoses are based on clinical criteria a …
They include Peutz-Jeghers syndrome, juvenile polyposis syndrome, the PTEN hamartoma tumor syndrome (including Cowden's syndrome and Bannaya …
Genomics of Hereditary Colorectal Cancer: Lessons Learnt from 25 Years of the Singapore Polyposis Registry.
Chew MH, Tan WS, Liu Y, Cheah PY, Loi CT, Tang CL. Chew MH, et al. Ann Acad Med Singap. 2015 Aug;44(8):290-6. Ann Acad Med Singap. 2015. PMID: 26477961 Free article. Review.
RESULTS: The registry currently has 253 families with several genetic conditions-93 familial adenomatous polyposis (FAP) families, 138 Amsterdam-criteria positive presumed Lynch syndrome (LS) families, 12 families with Peutz Jeghers syndrome, 2 families with Cowden's syndrome, an …
RESULTS: The registry currently has 253 families with several genetic conditions-93 familial adenomatous polyposis (FAP) families, 138 Amste …
17 results