Literature DB >> 10572557

Genetic testing for breast cancer predisposition.

M Gauthier-Villars1, S Gad, V Caux, S Pagès, C Blandy, D Stoppa-Lyonnet.   

Abstract

The recent identification of the BRCA1 and BRCA2 genes has improved our understanding of the association between breast and ovarian cancers in certain families. Carriers of predisposing germline mutations must decide on different options for management, including close follow-up or prophylactic surgery. Further studies are needed to elucidate the optimal management of these patients and to identify the factors that modify their risk for developing breast cancer. Finally, we must work to prevent any form of discrimination against those who, following genetic testing, are found to be at increased risk for breast cancer.

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Year:  1999        PMID: 10572557     DOI: 10.1016/s0039-6109(05)70067-0

Source DB:  PubMed          Journal:  Surg Clin North Am        ISSN: 0039-6109            Impact factor:   2.741


  2 in total

1.  Novel germline mutations in BRCA2 gene among 96 hereditary breast and breast-ovarian cancer families from Kerala, South India.

Authors:  Vani Syamala; Leelakumari Sreeja; Volga S Syamala; B Vinodkumar; Praveenkumar B Raveendran; Hariharan Sreedharan; Ratheesan Kuttappan; Lekshmi Balakrishnan; Ravindran Ankathil
Journal:  J Cancer Res Clin Oncol       Date:  2007-05-15       Impact factor: 4.553

2.  Cumulative BRCA mutation analysis in the Greek population confirms that homogenous ethnic background facilitates genetic testing.

Authors:  Alexandra Tsigginou; Fotios Vlachopoulos; Iordanis Arzimanoglou; Flora Zagouri; Constantine Dimitrakakis
Journal:  Hered Cancer Clin Pract       Date:  2015-08-19       Impact factor: 2.857

  2 in total

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