BRCA1 in the family: A case description of the psychological implications
- 11 July 1997
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
Abstract
Our experience with the first family in the Netherlands for whom predictive DNA-testing for Hereditary Breast and Ovarian Cancer (HBOC) became an option is described. This serves to illustrate the complex emotional impact on a family as a whole, and upon the members separately, of becoming aware that breast and ovarian cancer is hereditary, and the implications of undergoing predictive testing. All family members received genetic counseling and were offered pre- and post-test psychological follow-up. We observed two important roles within the family. One member became “the messenger of the news” informing the relatives of the hereditary character of cancer in the family. Another was “the first utilizer” of the new options; namely, the predictive DNA-test and preventive surgery. This first utilizer became the example to the rest of the family. Decisions made about preventive treatment (prophylactic ovariectomy and/or mastectomy) were based on the experiences within the family, whether one identified with an affected family member with breast or with ovarian cancer. The actions and reactions perceived were illustrative of what kind of support provisions should be provided in addition to the genetic and oncological counseling for HBOC. Moreover HBOC should be considered both as an individual and a family problem and be treated as such in genetic counseling. Am. J. Med. Genet. 71:63–71, 1997.Keywords
This publication has 34 references indexed in Scilit:
- Males at-risk for the BRCA1-gene, the psychological impactPsycho‐Oncology, 1996
- Women's receptivity to testing for a genetic susceptibility to breast cancer.American Journal of Public Health, 1995
- Rapid detection of BRCA1 mutations by the protein truncation testNature Genetics, 1995
- Age at diagnosis as an indicator of eligibility for BRCA1 DNA testing in familial breast cancerHuman Genetics, 1995
- Unusual case of Smith‐Lemli‐Opitz syndrome “type II”American Journal of Medical Genetics, 1995
- International Huntington Association and the World Federation of Neurology Research Group on Huntington's Chorea. Guidelines for the molecular genetics predictive test in Huntington's disease.Journal of Medical Genetics, 1994
- Familial cancer syndromesThe Lancet, 1994
- Risks of cancer in BRCA1-mutation carriersThe Lancet, 1994
- Predictive testing for Huntington disease in Canada: Adverse effects and unexpected results in those receiving a decreased riskAmerican Journal of Medical Genetics, 1992
- Psychological Distress and Surveillance Behaviors of Women With a Family History of Breast CancerJNCI Journal of the National Cancer Institute, 1992