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Small bowel polyposis syndromes.
Curr Gastroenterol Rep. 2011 Oct; 13(5):435-41.CG

Abstract

Intestinal polyposis syndromes are relatively rare. However, it is important for clinicians to recognize the potential risks of these syndromes. Based on histology, these syndromes can be classified mainly into hamartomatous polyposis syndromes and familial adenomatous polyposis (FAP), which affects mainly the large intestine. This review discusses the clinical manifestations and underlying genetics of the most common small intestinal polyposis syndromes: Peutz-Jeghers syndrome (PJS), juvenile polyposis (JP), PTEN hamartoma tumor syndrome (PHTS), and the small intestinal implications of familial adenomatous polyposis (FAP).

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Authors+Show Affiliations

Arber N
Integrated Cancer Prevention Center, Tel Aviv Sourasky Medical Center, 6 Weizmann St., Tel Aviv 64239, Israel. nadira@tasmc.health.gov.il
Moshkowitz M
No affiliation info available

MeSH

Adenomatous Polyposis ColiHamartoma Syndrome, MultipleHumansIntestinal PolyposisNeoplastic Syndromes, HereditaryPeutz-Jeghers SyndromePrecancerous Conditions

Pub Type(s)

Journal Article
Review

Language

eng

PubMed ID

21800071

Citation

Arber, Nadir, and Menachem Moshkowitz. "Small Bowel Polyposis Syndromes." Current Gastroenterology Reports, vol. 13, no. 5, 2011, pp. 435-41.
Arber N, Moshkowitz M. Small bowel polyposis syndromes. Curr Gastroenterol Rep. 2011;13(5):435-41.
Arber, N., & Moshkowitz, M. (2011). Small bowel polyposis syndromes. Current Gastroenterology Reports, 13(5), 435-41. https://doi.org/10.1007/s11894-011-0218-4
Arber N, Moshkowitz M. Small Bowel Polyposis Syndromes. Curr Gastroenterol Rep. 2011;13(5):435-41. PubMed PMID: 21800071.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Small bowel polyposis syndromes. AU - Arber,Nadir, AU - Moshkowitz,Menachem, PY - 2011/7/30/entrez PY - 2011/7/30/pubmed PY - 2012/1/27/medline SP - 435 EP - 41 JF - Current gastroenterology reports JO - Curr Gastroenterol Rep VL - 13 IS - 5 N2 - Intestinal polyposis syndromes are relatively rare. However, it is important for clinicians to recognize the potential risks of these syndromes. Based on histology, these syndromes can be classified mainly into hamartomatous polyposis syndromes and familial adenomatous polyposis (FAP), which affects mainly the large intestine. This review discusses the clinical manifestations and underlying genetics of the most common small intestinal polyposis syndromes: Peutz-Jeghers syndrome (PJS), juvenile polyposis (JP), PTEN hamartoma tumor syndrome (PHTS), and the small intestinal implications of familial adenomatous polyposis (FAP). SN - 1534-312X UR - https://www.unboundmedicine.com/medline/citation/21800071/Small_bowel_polyposis_syndromes_ L2 - https://dx.doi.org/10.1007/s11894-011-0218-4 DB - PRIME DP - Unbound Medicine ER -