نتایج جستجو برای: familial polyposis coli

تعداد نتایج: 208445  

2017
Bente A. Talseth-Palmer

Colorectal cancer (CRC) is one of the most common forms of cancer worldwide and familial adenomatous polyposis (FAP) accounts for approximately 1% of all CRCs. Adenomatous polyposis syndromes can be divided into; familial adenomatous polyposis (FAP) - classic FAP and attenuated familial adenomatous polyposis (AFAP), MUTYH-associated polyposis (MAP), NTHL1-associated polyposis (NAP) and polymera...

Journal: :The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology 2005
Cüneyt Kayaalp Sevil Işik Soner Akbaba Gürel Neşşar Erkan Oymaci Canbek Seven

The aim of this study was to assess whether restorative proctocolectomy was suitable as an initial procedure for selected familial adenomatous polyposis patients with coexisting colorectal cancer. Six malignancy patients who underwent restorative proctocolectomy for familial adenomatous polyposis were reviewed. At the time of restorative proctocolectomy, cancer was not suspected in four patient...

Journal: :Cancer research 2001
K Heinimann A Thompson A Locher T Furlanetto E Bader A Wolf R Meier K Walter P Bauerfeind G Marra H Müller D Foernzler Z Dobbie

Familial adenomatous polyposis, an autosomal-dominantly inherited colorectal cancer predisposition syndrome, is caused by germ-line mutations in the adenomatous polyposis coli (APC) gene. Despite the use of different screening methods, studies worldwide fail to identify APC mutations in 20-50% of all familial adenomatous polyposis patients (APC mutation-negatives). In this study, missense mutat...

2008
S. A. R. COOKE

the inherited polyposis syndromes and colorectal carcinoma. Four patients are reported, to illustrate the wide spectrum of colonic polyps which may occur in multiple form in adults. Included are unusual cases of metaplastic and-juvenile polyposis. The subject is reviewed, and the need for accurate histological diagnosis is stressed. The possibility that the difference between familial adenomato...

Journal: :Clinical genetics 2012
C Mongin F Coulet J H Lefevre C Colas M Svrcek M Eyries Y Lahely J-F Fléjou F Soubrier Y Parc

Two main colorectal polyposis syndromes have been described, familial adenomatous polyposis and MUTYH-associated polyposis syndromes. Some polyposis remains unexplained: 20% of adenomatous polyposis and serrated polyposis. The aim of this study was to evaluate in a cohort of patients with unexplained polyposis whether a genetic defect could be detected. Individuals presenting polyposis with mor...

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