نتایج جستجو برای: Adenomatous Polyposis Coli

تعداد نتایج: 158575  

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 ...

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: :journal of minimally invasive surgical sciences 0
fabio guilherme campos corresponding author: fabio guilherme campos, gastroenterology department, colorectal unit, hospital das clinicas, medical school, university of sao paulo, brazil ; corresponding author: fabio guilherme campos, gastroenterology department, colorectal unit, hospital das clinicas, medical school, university of sao paulo, brazil

Journal: :international journal of pediatrics 0
manoochehr karjoo department of pediatric gastroenterology, hepatology and nutrition, golisano children hospital, upstate medical university, syracuse new york, usa. qurratul ann warsi department of epidemiology and biostatistics, university of california and san francisco, san francisco, california, usa. devin halleran department of pediatric gastroenterology, hepatology and nutrition, golisano children hospital, upstate medical university, syracuse new york, usa. marcus rivera department of pediatric gastroenterology, hepatology and nutrition, golisano children hospital, upstate medical university, syracuse new york, usa.

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 been...

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...

Background: Deep vein thrombosis is an important cause of morbidity and mortality. However, its association with adenomatous polyposis coli is extremely rare. Here we present an interesting case of deep vein thrombosis associated with adenomatous polyposis coli. Case Presentation: A 15 year old female who was having fever and diarrhea for 5 months developed bilateral asymmetric painful swell...

Journal: :international journal of molecular and cellular medicine 0
seyed mohammad hossein kashfi gastroenterology and liver diseases research center, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) faegheh behboudi farahbakhsh basic and molecular epidemiology of gastrointestinal disorders research center, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) mina golmohammadi basic and molecular epidemiology of gastrointestinal disorders research center, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) ehsan nazemalhosseini mojarad gastroenterology and liver diseases research center, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) pedram azimzadeh gastroenterology and liver diseases research center, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) hamid asadzadeh aghdaie basic and molecular epidemiology of gastrointestinal disorders research center, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences)

familial adenomatous polyposis (fap) is responsible for < 1% of colorectal cancer (crc) cases and is inherited as an autosomal dominant trait. patients generally present hundreds to thousands of adenomas and develop colorectal cancer by age 35- 40 if left untreated. here we report four patients with germline frameshift mutation (small deletion) at exon 15 of adenomatous polyposis coli (apc) tum...

Journal: :caspian journal of internal medicine 0
neha agrawal department of medicine, calcutta national medical college and hospital, kolkata, india tuhin santra department of medicine, calcutta national medical college and hospital, kolkata, india arnab kar . department of medicine, gangarampur subdivisional hospital, india pradipta guha department of medicine, calcutta national medical college and hospital, kolkata, india mita bar kolkata, india apu adhikary department of medicine, north bengal medical college &amp; hospital, india

background: deep vein thrombosis is an important cause of morbidity and mortality. however, its association with adenomatous polyposis coli is extremely rare. here we present an interesting case of deep vein thrombosis associated with adenomatous polyposis coli. case presentation: a 15 year old female who was having fever and diarrhea for 5 months developed bilateral asymmetric painful swelling...

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: :Cancer research 1993
M Miyaki M Konishi R Kikuchi-Yanoshita M Enomoto K Tanaka H Takahashi M Muraoka T Mori F Konishi T Iwama

Desmoid tumors, which are locally invasive with recurrence but without metastasis, are frequently observed in patients with familial adenomatous polyposis after abdominal surgery or during pregnancy. This study analyzed mutation of the adenomatous polyposis coli gene in 8 desmoid tumors from 7 familial adenomatous polyposis patients using polymerase chain reaction-single-strand conformation pol...

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