Individuals who carry an inherited mutation in the breast cancer 1 (BRCA1) and BRCA2 genes have a significant risk of developing breast and ovarian cancer over the course of their lifetime. As a result, there are important considerations for the clinician in the counseling, followup and management of mutation carriers. This review outlines salient aspects in the approach to patients at high risk of developing breast and ovarian cancer, including criteria for genetic testing, screening guidelines, surgical prophylaxis, and chemoprevention.
Clinical Considerations of BRCA1- and BRCA2-Mutation Carriers: A Review
Published 2011 in International Journal of Surgical Oncology
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- Publication year
2011
- Venue
International Journal of Surgical Oncology
- Publication date
2011-08-08
- Fields of study
Medicine
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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