Literature DB >> 18006790

New issues in genetic counseling of hereditary colon cancer.

Patrick M Lynch1.   

Abstract

Clinicians face significant challenges in the diagnosis and management of familial colorectal cancer predisposition. Many of the challenges concern the rarity of individual conditions and their unfamiliarity to most clinicians, even those in the subspecialty areas of gastroenterology, colorectal surgery, and medical oncology. Because the World Wide Web now offers a wealth of information, familiarity with available online resources should be a minimal expectation of clinicians. Notably, these same resources are available to the lay public, so a more informed group of patients can be expected and is already being encountered. The web sites noted throughout this article are merely early examples of what should become an opportunity for instant access to the most up-to-date knowledge of rare familial colorectal cancers and their clinical features, molecular diagnostics, and clinical management and prevention. Many professional organizations have produced guidelines (in print and online) for use by practitioners in various specialties. The consistency, growing evidence base, and ready availability of these guidelines to providers and patients alike will likely foster greater recognition of the need to be in compliance with them. Finally, as investigators make progress with the genetics of these rare diseases, one can anticipate a "cooperative group" approach to clinical trials.

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Year:  2007        PMID: 18006790     DOI: 10.1158/1078-0432.CCR-07-1124

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  4 in total

1.  Sharing genetic risk with next generation: mutation-positive parents' communication with their offspring in Lynch Syndrome.

Authors:  Katja I Aktan-Collan; Helena A Kääriäinen; Eeva M Kolttola; Kirsi Pylvänäinen; Heikki J Järvinen; Ari H Haukkala; Jukka-Pekka Mecklin
Journal:  Fam Cancer       Date:  2011-03       Impact factor: 2.375

2.  Limited impact on self-concept in individuals with Lynch syndrome; results from a national cohort study.

Authors:  Helle Vendel Petersen; Mary Jane Esplen; Steen Ladelund; Inge Bernstein; Lone Sunde; Christina Carlsson; Mef Nilbert
Journal:  Fam Cancer       Date:  2011-12       Impact factor: 2.375

3.  Ultradeep sequencing of a human ultraconserved region reveals somatic and constitutional genomic instability.

Authors:  Anna De Grassi; Cinzia Segala; Fabio Iannelli; Sara Volorio; Lucio Bertario; Paolo Radice; Loris Bernard; Francesca D Ciccarelli
Journal:  PLoS Biol       Date:  2010-01-05       Impact factor: 8.029

4.  Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels.

Authors:  Katarina Domanska; Christina Carlsson; Pär-Ola Bendahl; Mef Nilbert
Journal:  BMC Med Genet       Date:  2009-03-26       Impact factor: 2.103

  4 in total

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