A new mutation in Muir-Torre syndrome associated with familiar transmission of different gastrointestinal adenocarcinomas

Abstract Hereditary Nonpolyposis Colorectal Carcinoma (HNPCC) is the most frequent inherited disease which can lead to the development of tumors in the colon and other locations. Its genetic basis is related to the germline mutation of the Mismatch Repair (MMR) genes. Muir-Torre syndrome is consider...

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Veröffentlicht in:	European journal of surgical oncology 2009-10, Vol.35 (10), p.1128-1130
Hauptverfasser:	Tanyi, M, Olasz, J, Lukács, G, Tanyi, J.L, Tóth, L, Antal-Szalmás, P, Ress, Z, Bubán, T, András, C, Damjanovich, L
Format:	Artikel
Sprache:	eng
Schlagworte:	Adaptor Proteins, Signal Transducing - genetics Adenocarcinoma, Mucinous - genetics Adenocarcinoma, Mucinous - pathology Cecal Neoplasms - genetics Cecal Neoplasms - pathology Family Health Hematology, Oncology and Palliative Medicine Hereditary nonpolyposis colorectal cancer hMLH1 hMSH2 Humans Male Middle Aged Muir-Torre syndrome Muir-Torre Syndrome - genetics Muir-Torre Syndrome - pathology Mutation Mutation, Missense MutL Protein Homolog 1 MutL Proteins Neoplasm Proteins - genetics Nuclear Proteins - genetics Pancreatic Neoplasms - genetics Pancreatic Neoplasms - pathology Pedigree Surgery
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