Genetic/Familial High-Risk Assessment: Breast and Ovarian

  • Daly M
  • Axilbund J
  • Buys S
  • et al.
N/ACitations
Citations of this article
398Readers
Mendeley users who have this article in their library.

Abstract

All cancers develop as a result of mutations in certain genes, such as those involved in the regulation of cell growth and/or DNA repair, but not all mutations are inherited. However, family studies have long documented an increased risk for several forms of cancer among first and second-degree relatives . Hereditary cancers are often characterized by mutations associated with a high probability of cancer development, vertical transmission through either mother or father, and an association with other types of tumors. They often have an early age of onset and exhibit an autosomal dominant inheritance pattern. Familial cancers share only some features of hereditary cancers. Although other cancers are associated with these hereditary syndromes, these guidelines mainly focus on management of breast and ovarian cancer risk in these individuals. (copyright) Journal of the National Comprehensive Cancer Network.

Cite

CITATION STYLE

APA

Daly, M. B., Axilbund, J. E., Buys, S., Crawford, B., Farrell, C. D., Friedman, S., … Weitzel, J. N. (2017). Genetic/Familial High-Risk Assessment: Breast and Ovarian. Journal of the National Comprehensive Cancer Network, 8(5), 562–594. https://doi.org/10.6004/jnccn.2010.0043

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free