Actes anteriors
Identification and characterization of Lynch syndrome: contributions of the EPICOLON project
Speaker: Antoni Castells, MD
Gastroenterology Service, Hospital Clínic
Barcelona, Spain
Host
Roger Gomis, IRB Barcelona
Friday, 27 June 2008, 12.00h Aula Fèlix Serratosa
Abstract
Lynch syndrome, also known as hereditary non-polyposis colorectal cancer, is the most common form of hereditary colorectal cancer. It is characterized by early onset of colorectal cancer and other extracolonic associated malignancies. This disorder is inherited in an autosomal dominant pattern and is due to mutations in the DNA-mismatch repair genes. The EPICOLON study, a prospective, multicenter, nation-wide, population-based epidemiological project, lead by the Spanish Gastroenterological Association, has contributed to the clinical and molecular characterization of this syndrome.









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