نتایج جستجو برای: lynch syndrome

تعداد نتایج: 623651  

Journal: :Oncology reports 2016
Kristina Lagerstedt-Robinson Anna Rohlin Christos Aravidis Beatrice Melin Margareta Nordling Marie Stenmark-Askmalm Annika Lindblom Mef Nilbert

Lynch syndrome caused by constitutional mismatch‑repair defects is one of the most common hereditary cancer syndromes with a high risk for colorectal, endometrial, ovarian and urothelial cancer. Lynch syndrome is caused by mutations in the mismatch repair (MMR) genes i.e., MLH1, MSH2, MSH6 and PMS2. After 20 years of genetic counseling and genetic testing for Lynch syndrome, we have compiled th...

2003
H K Roy H T Lynch

R isk stratification is essential for designing efficacious and cost effective colon cancer screening programmes. One of the most important risk factors for colorectal cancers (CRC) is an inherited predisposition, implicated in 20% of all cases. The spectrum of genetic susceptibility ranges from the low penetrance mutations that modestly increase the colon cancer risk (for example, I 1307K) to ...

Journal: :Hereditary Cancer in Clinical Practice 2008
Józef Kładny Jan Lubiński

Lynch syndrome, also referred to as hereditary non-polyposis colorectal cancer (HNPCC), accounts for somewhere between 2 and 5% of all CRC. It has been shown that Lynch syndrome (LS) is a result of germline mutations in genes involved in DNA mismatch repair (MMR) MSH2, MLH1, MSH6, and PMS2, whereas as HNPCC refers to families that adhere to the Amsterdam criteria or iterations of it. More recen...

2013
Eun Jin Heo Jung Min Park Eun Hee Lee Hyoun Wook Lee Min Kyu Kim

Lynch syndrome is a genetic malignancy syndrome affecting the colon, endometrium, and other organs. It is difficult to find a Lynch syndrome patient without any family history of cancer. We have recently examined an endometrial cancer patient with a MSH2 gene mutation without a family history of cancer. A 55-year old Korean woman was admitted to a local clinic for vaginal bleeding. An endometri...

2017
Sanja Kapitanović

Colorectal cancer (CRC) is one of the most common cancers and one of the leading causes of cancer death in the Western world. The disease arises from the accumulation of mutations in oncogenes, tumor suppressor genes and mismatch repair genes during progression from normal colon epithelium to adenoma and metastatic carcinoma. The majority of colorectal cancers arise in sporadic form. About one-...

Journal: :Human mutation 2011
Roland P Kuiper Lisenka E L M Vissers Ramprasath Venkatachalam Danielle Bodmer Eveline Hoenselaar Monique Goossens Aline Haufe Eveline Kamping Renée C Niessen Frans B L Hogervorst Johan J P Gille Bert Redeker Carli M J Tops Marielle E van Gijn Ans M W van den Ouweland Nils Rahner Verena Steinke Philip Kahl Elke Holinski-Feder Monika Morak Matthias Kloor Susanne Stemmler Beate Betz Pierre Hutter David J Bunyan Sapna Syngal Julie O Culver Tracy Graham Tsun L Chan Iris D Nagtegaal J Han J M van Krieken Hans K Schackert Nicoline Hoogerbrugge Ad Geurts van Kessel Marjolijn J L Ligtenberg

Recently, we identified 3' end deletions in the EPCAM gene as a novel cause of Lynch syndrome. These truncating EPCAM deletions cause allele-specific epigenetic silencing of the neighboring DNA mismatch repair gene MSH2 in tissues expressing EPCAM. Here we screened a cohort of unexplained Lynch-like families for the presence of EPCAM deletions. We identified 27 novel independent MSH2-deficient ...

Journal: :World Journal of Surgical Oncology 2008
Frederik J Hes

BACKGROUND Germ line mutations in mismatch repair genes underlie Lynch syndrome and predispose carriers for colorectal carcinoma and malignancies in many other organ systems. CASE PRESENTATION A large Lynch syndrome family with 15 affected family members and involvement in 7 organs is reported. It illustrates a lack of awareness and knowledge about this hereditary tumor syndrome among doctors...

2015
Steven Sorscher

Patients with Lynch Syndrome are at high risk for developing a variety of cancers including cancers of the colon or rectum, small bowel, stomach, uterus, renal pelvis, ureter, biliary tract, ovaries, brain and pancreas (N Engl J Med 348: 919-32, 2003; Gut 57:1097-101, 2008; NCCN, Inc Guideline. Ft. Washington, PA. Online Version 2.2014). Lack of MLH-1 and MSH-2 expression commonly result from g...

2013
Nuria Seguí Marta Pineda Elisabet Guinó Ester Borràs Matilde Navarro Fernando Bellido Victor Moreno Conxi Lázaro Ignacio Blanco Gabriel Capellá Laura Valle

Telomere length variation has been associated with increased risk of several types of tumors, and telomere shortening, with genetic anticipation in a number of genetic diseases including hereditary cancer syndromes. No conclusive studies have been performed for Lynch syndrome, a hereditary colorectal cancer syndrome caused by germline mutations in the DNA mismatch repair genes. Here we evaluate...

2011
Cristina Bozzao Patrizia Lastella Alessandro Stella

Lynch syndrome (LS) is the most common form of inherited predisposition to develop cancer mainly in the colon and endometrium but also in other organ sites. Germline mutations in DNA mismatch repair (MMR) gene cause the transmission of the syndrome in an autosomal dominant manner. The management of LS patients is complicated by the large variation in age at cancer diagnosis which requires these...

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