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1.
J Genet Couns ; 18(2): 160-72, 2009 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-19219540

RESUMO

Although the discovery of mutations on BRCA1 and BRCA2 genes associated with high breast cancer risk has given rise to screening and surveillance initiatives, there is little documentation on why high-risk women choose to enter screening programs. The objective of this qualitative study was to develop a detailed understanding of the experiences and decisions that motivate women with increased risk of hereditary breast cancer to participate in the multicentered Quebec experimental breast screening program. Our study involved 21 participants who were either BRCA carriers or at risk and untested. These women were interviewed while participating in the screening program. Our study demonstrates that intensive screening programs may provide valuable reassurance for women with increased familial risk of hereditary breast cancer, who count on early detection and rapid response from professionals if and when a problem arises. Health professionals must take these and others concerns into account to ensure their interventions are most consistent with women's needs.


Assuntos
Neoplasias da Mama/genética , Predisposição Genética para Doença , Testes Genéticos/psicologia , Feminino , Genes BRCA1 , Genes BRCA2 , Humanos , Quebeque
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