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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Bradbury, Angela R. Patrick-Miller, Linda Pawlowski, Kimberly Ibe, Comfort N. Cummings, Shelly A. Olopade, Olufunmilayo I. Daugherty, Christopher K. |
| Description | Country affiliation: United States Author Affiliation: Bradbury AR ( Fox Chase Cancer, Division of Population Science, Philadelphia, PA 19111, USA. angela.bradbury@fccc.edu) |
| Abstract | Although professional guidelines recommend against testing minors for adult-onset genetic conditions, the genetic testing of minors for BRCA1/2 alterations has been debated in the literature. To better understand the opinions of BRCA mutation carriers regarding the genetic testing of minors and the cognitive and affective processes underlying these opinions, we interviewed BRCA mutation carriers and their adult offspring who had learned of their parent's BRCA mutation. Semi-structured interviews were conducted with 53 parents and 22 offspring. In response to a closed-ended question, 52% (n = 39) of participants were opposed to the testing of minors. Responses to an open-ended question indicate that many participants (24%, n = 18) feel that testing could be permitted for some minor offspring. Psychological risks and the insufficient maturity of minors were frequent concerns of participants opposed to testing minors. The potential to impact health behaviors was frequently cited as a reason to support the genetic testing of minors. These preliminary results suggest that many BRCA mutation carriers and their adult offspring have concerns about, or are opposed to the genetic testing of minors. However, a significant minority in our study would support testing minors. Greater support for testing among offspring could indicate increasing requests for early genetic diagnosis. Further research is necessary to explore the risks and benefits of providing genetic testing to minors for adult-onset hereditary cancer syndromes in order to inform clinical practice and public policy and to ensure optimal psychosocial and medical outcomes for all members in families at risk for genetically determined disease. |
| File Format | HTM / HTML |
| ISSN | 15524868 |
| Issue Number | 1 |
| Volume Number | 148C |
| e-ISSN | 15524876 |
| Journal | American Journal of Medical Genetics Part C: Seminars in Medical Genetics |
| Language | English |
| Publisher | Wiley |
| Publisher Date | 2008-02-15 |
| Publisher Place | United States |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Discipline Genetics Discipline Medical Genes, Brca1 Genes, Brca2 Genetic Testing Ethics Heterozygote Mutation Adolescent Adult Cohort Studies Data Collection Female Humans Interviews As Topic Pedigree Journal Article Research Support, Non-u.s. Gov't |
| Content Type | Text |
| Resource Type | Article |
| Subject | Genetics Genetics (clinical) |
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