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Genetic Counselling and Testing for Hereditary Breast and Ovarian Cancer: The Gent(le) Approach

The counselling experience with 50 Flemish families in whom mutation analysis of the total coding region of the BRCA1 and BRCA2 gene has been initiated, is presented. Genetic testing for breast-ovarian cancer susceptibility is offered by a multidisciplinary team. During the counselling sessions, spe...

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Detalles Bibliográficos
Autores principales: De Vos, M., Poppe, B., Delvaux, I., Mortier, G., Claes, K., Messiaen, L., De Paepe, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850851/
https://www.ncbi.nlm.nih.gov/pubmed/10595277
http://dx.doi.org/10.1155/1999/809125
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author De Vos, M.
Poppe, B.
Delvaux, I.
Mortier, G.
Claes, K.
Messiaen, L.
De Paepe, A.
author_facet De Vos, M.
Poppe, B.
Delvaux, I.
Mortier, G.
Claes, K.
Messiaen, L.
De Paepe, A.
author_sort De Vos, M.
collection PubMed
description The counselling experience with 50 Flemish families in whom mutation analysis of the total coding region of the BRCA1 and BRCA2 gene has been initiated, is presented. Genetic testing for breast-ovarian cancer susceptibility is offered by a multidisciplinary team. During the counselling sessions, special attention is given to comprehensible and emotionally acceptable communi-cation of genetic information and to the psychosocial evaluation of the counselee. The limitations of molecular testing and the controversy surrounding cancer prevention strategies are also discussed. The overall acceptance of mutation testing is high. Some of the problems encountered are inaccuracy of the reported family history, poor retrieval of the medical records of affected family members and the reluctance of many patients to inform their relatives about the possibility of being tested.
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spelling pubmed-38508512013-12-18 Genetic Counselling and Testing for Hereditary Breast and Ovarian Cancer: The Gent(le) Approach De Vos, M. Poppe, B. Delvaux, I. Mortier, G. Claes, K. Messiaen, L. De Paepe, A. Dis Markers Other The counselling experience with 50 Flemish families in whom mutation analysis of the total coding region of the BRCA1 and BRCA2 gene has been initiated, is presented. Genetic testing for breast-ovarian cancer susceptibility is offered by a multidisciplinary team. During the counselling sessions, special attention is given to comprehensible and emotionally acceptable communi-cation of genetic information and to the psychosocial evaluation of the counselee. The limitations of molecular testing and the controversy surrounding cancer prevention strategies are also discussed. The overall acceptance of mutation testing is high. Some of the problems encountered are inaccuracy of the reported family history, poor retrieval of the medical records of affected family members and the reluctance of many patients to inform their relatives about the possibility of being tested. IOS Press 1999 2002-06-07 /pmc/articles/PMC3850851/ /pubmed/10595277 http://dx.doi.org/10.1155/1999/809125 Text en Copyright © 1999 Hindawi Publishing Corporation.
spellingShingle Other
De Vos, M.
Poppe, B.
Delvaux, I.
Mortier, G.
Claes, K.
Messiaen, L.
De Paepe, A.
Genetic Counselling and Testing for Hereditary Breast and Ovarian Cancer: The Gent(le) Approach
title Genetic Counselling and Testing for Hereditary Breast and Ovarian Cancer: The Gent(le) Approach
title_full Genetic Counselling and Testing for Hereditary Breast and Ovarian Cancer: The Gent(le) Approach
title_fullStr Genetic Counselling and Testing for Hereditary Breast and Ovarian Cancer: The Gent(le) Approach
title_full_unstemmed Genetic Counselling and Testing for Hereditary Breast and Ovarian Cancer: The Gent(le) Approach
title_short Genetic Counselling and Testing for Hereditary Breast and Ovarian Cancer: The Gent(le) Approach
title_sort genetic counselling and testing for hereditary breast and ovarian cancer: the gent(le) approach
topic Other
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850851/
https://www.ncbi.nlm.nih.gov/pubmed/10595277
http://dx.doi.org/10.1155/1999/809125
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