نتایج جستجو برای: familial polyposis coli

تعداد نتایج: 208445  

Journal: :acta medica iranica 0
sanambar sadighi department of medical oncology, cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran. mahsa ghaffari-moghaddam department of medical genetics, cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran. mojtaba saffari department of medical genetics, cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran. and departement of medical genetics, school of medicine, tehran university of medical genetics, tehran, iran. mohammad ali mohagheghi department of surgical oncology, cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran. reza shirkoohi department of medical genetics, cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran

desmoids tumors, characterized by monoclonal proliferation of myofibroblasts, could occur in 5-10% of patients with familial adenomatous polyposis (fap) as an extra-colonic manifestation of the disease. fap can develop when there is a germ-line mutation in the adenomatous polyposis coli gene. although mild or attenuated fap may follow mutations in 5΄ extreme of the gene, it is more likely that ...

Journal: :gastroenterology and hepatology from bed to bench 0
seyed mohammad hossein kashfi basic and molecular epidemiology of gastroenterology disorders research center, shahid beheshti university of medical sciences, tehran, iran mina golmohammadi basic and molecular epidemiology of gastroenterology disorders research center, shahid beheshti university of medical sciences, tehran, iran faeghe behboudi basic and molecular epidemiology of gastroenterology disorders research center, shahid beheshti university of medical sciences, tehran, iran ehsan nazemalhosseini- mojarad gastroenterology and liver diseases research center, shahid beheshti university of medical science, tehran, iran mohammad reza zali gastroenterology and liver diseases research center, shahid beheshti university of medical science, tehran, iran

normal 0 false false false en-us x-none ar-sa microsoftinternetexplorer4 colorectal cancer is classified in to three forms: sporadic (70-75%), familial (20-25%) and hereditary (5-10%). hereditary colorectal cancer syndromes classified into two different subtypes: polyposis and non polyposis. familial adenomatous polyposis (fap; omim #175100) is the most common polyposis syndrome, account for <1...

Ashraf Mohamadkhani, Maliheh Moradzadeh, Mehrdad Aghaei, Mohammad Hassan Jokar, Sima Sedighi,

Familial adenomatous polyposis is characterized by over 100 colorectal adenomas in the colorectum. The disease equally affects both sexes, with an incidence estimated at 1.14025-1.8300. The disease is premature in people with familial adenomatous polyposis. Patients suffering from familial adenomatous polyposis have a range of extra-intestinal diseases such as papillae, gastric, small intestine...

Journal: :iranian journal of pathology 0
mitra heidarpour dept. of pathology, isfahan university of medical sciences, isfahan, iran farzaneh sajjadi . dept. of pathology, isfahan university of medical sciences, isfahan, iran seyed abass tabatabai dept. of surgery, isfahan university of medical sciences, isfahan, iran majid heidarpour dept. of orthodontics, shahid beheshti university of medical sciences, tehran, iran

gardner&apos;s syndrome is an autosomal dominant inherited disorder. familial polyposis of the colon, osteomas, hypertrophy of the retinal-pigmented layer and a multitude of soft tissue tumors are characteristic features. the syndrome may be presented with colonic or extracolonic symptoms. a 75-year-old male patient presented to al-zahra clinic with diffuse abdominal pain. an abdominal surgery ...

Journal: :iranian journal of pathology 2010
mitra heidarpour farzaneh sajjadi seyed abass tabatabai majid heidarpour

gardner's syndrome is an autosomal dominant inherited disorder. familial polyposis of the colon, osteomas, hypertrophy of the retinal-pigmented layer and a multitude of soft tissue tumors are characteristic features. the syndrome may be presented with colonic or extracolonic symptoms. a 75-year-old male patient presented to al-zahra clinic with diffuse abdominal pain. an abdominal surgery was p...

Journal: :British Journal of Cancer 1976

Journal: :JOP : Journal of the pancreas 2008
Alaa Elkharwily Klaus Gottlieb

Familial adenomatous polyposis is an archetypal disease illustrating the genetic basis of human cancer. The adenomatous polyposis coli gene functions as a tumor suppressor with hundreds of known mutations that result in a defective adenomatous polyposis coli protein. In addition to the certain fate of colon cancer without colectomy, patients with familial adenomatous polyposis are also at incre...

Journal: :Gastroenterology 1982

Journal: :Journal of the Belgian Society of Radiology 2011

     Familial adenomatous polyposis (FAP) is a hereditary autosomal dominant cancer syndrome, results from germ line mutation or deletion of the Adenomatous Polyposis Coli (APC) gene on chromosome 5q21. Patients with FAP suffer from multiple polyps mainly at the colorectal region as well as other parts of the gastrointestinal tract, which has propensity to transform into carcinoma. FAP has also...

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