نتایج جستجو برای: hereditary cancer syndrome

تعداد نتایج: 1562314  

Journal: :Onkourologiâ 2023

Renal cell carcinoma is one of the most common malignant neoplasms genitourinary system. Along with smoking and hereditary syndromes associated mutations in Von Hippel-Lindau (VHL) gene, obesity main risk factors for development renal carcinoma. Emerging data indicate a causal relationship between In large study within framework Metabolic Syndrome Cancer project, clinical on blood pressure, bod...

Journal: :Seminars in cutaneous medicine and surgery 2012
Vasiliki Nikolaou Alexander J Stratigos Hensin Tsao

Cutaneous basal and squamous cell carcinomas are among the most frequent malignancies in the white population, with the annual incidence estimates ranging from 1 million to 3.5 million cases in the United States. These tumors can occur either sporadically or in the context of hereditary genodermatoses with cancer predisposition, such as basal cell nevus syndrome, xeroderma pigmentosum, epidermo...

Journal: :Oncology nursing forum 2011
Suzanne M Mahon

641 O ncology is one of the first subspecialties to experience the full impact of the genomics revolution; oncology nurses regularly use genomic science in prevention, screening, diagnostics, prognostics, selection of treatment, and monitoring of treatment effectiveness in cancer care (Mahon, 2009). Genetic tests are now routinely ordered to determine risk for developing and appropriate managem...

2010
A.P. Sokolenko A.G. Iyevleva N.V. Mitiushkina E.N. Suspitsin E.`V. Preobrazhenskaya E.Sh. Kuligina D.A. Voskresenskiy O.S. Lobeiko N.Yu. Krylova T.V. Gorodnova K.G. Buslov E.M. Bit-Sava G.D. Dolmatov N.V. Porhanova I.S. Polyakov S.N. Abysheva A.S. Katanugina D.V. Baholdin G.A. Yanus A.V. Togo V.M. Moiseyenko S.Ya. Maximov V.F. Semiglazov E.N. Imyanitov

Hereditary breast-ovarian cancer syndrome contributes to as much as 5-7% of breast cancer (BC) and 10-15% of ovarian cancer (OC) incidence. Mutations in the "canonical" genesBRCA1andBRCA2occur in 20-30% of affected pedigrees. In addition toBRCA1andBRCA2 mutations, germ-line lesions in theCHEK2,NBS1, andPALB2genes also contribute to familial BC clustering. The epidemiology of hereditary breast-o...

Journal: :medical journal of islamic republic of iran 0
shirzad nasiri tehran university of medical sciences. address: general surgery ward,shariati hospital, north kargar st. tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences)سازمان های دیگر: ,shariati hospital anushiravan hedayat tehran university of university of medical sciencesسازمان اصلی تایید شده: دانشگاه تهران (tehran university) reza malekzadeh tehran university of medical sciencesسازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) zhamak khorgami tehran university of medical sciencesسازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) nassim sodagari tehran university of medical sciencesسازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences)

absract gastric cancer is the fourth most common cancer and the second leading cause of cancer death. most cases are sporadic and only 10% of patients, show familial clustering. among these patients, 1 to 3 % have hereditary diffuse gastric cancer (hdgc), which is autosomal-dominant and present in younger ages. mutations in ecadherin gene cdh1 has been identified in 30 to 50% of patients. becau...

Journal: :Oncology Reviews 2023

Both cancer and metabolic disease have become the prevalent health risks in modern societies worldwide. Cancer is a complex set of illnesses with many definitions. About 15% cancers are caused by infections, 10% carry hereditary burden. The remaining 70%–75% associated variety processes, often syndrome chronic inflammation. This review examines role dysfunction inflammation development. I propo...

Journal: :Journal of the National Cancer Institute 2007
Kristina Lagerstedt Robinson Tao Liu Jana Vandrovcova Britta Halvarsson Mark Clendenning Thierry Frebourg Nickolas Papadopoulos Kenneth W Kinzler Bert Vogelstein Päivi Peltomäki Richard D Kolodner Mef Nilbert Annika Lindblom

BACKGROUND Preventive programs for individuals who have high lifetime risks of colorectal cancer may reduce disease morbidity and mortality. Thus, it is important to identify the factors that are associated with hereditary colorectal cancer and to monitor the effects of tailored surveillance. In particular, patients with Lynch syndrome, hereditary nonpolyposis colorectal cancer (HNPCC), have an...

Journal: :Deutsches Arzteblatt international 2013
Verena Steinke Christoph Engel Reinhard Büttner Hans Konrad Schackert Wolff H Schmiegel Peter Propping

BACKGROUND Hereditary nonpolyposis colorectal cancer HNPCC, Lynch syndrome) is a genetic disease of autosomal dominant inheritance. It is caused by a mutation in one of four genes of the DNA mismatch repair system and confers a markedly increased risk for various types of cancer, particularly of the colon and the endometrium. Its prevalence in the general population is about 1 in 500, and it ca...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید