Disease markers · 1999
Genetic counselling and testing for hereditary breast and ovarian cancer: the gent(le) approach.
Клинический случайСтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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De Vos M, Poppe B, Delvaux I, Mortier G, Claes K, Messiaen L, De Paepe A
Аннотация
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 communication 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.
Предметные рубрики MeSH
AdultAge of OnsetBRCA2 ProteinBelgiumBreast NeoplasmsDNA Mutational AnalysisEndometrial NeoplasmsFamily HealthFemaleGenes, BRCA1Genetic CounselingGenetic TestingHumansMiddle AgedNeoplasm ProteinsOncogenesOvarian NeoplasmsPatient Care TeamPatient Education as TopicPolymerase Chain ReactionPredictive Value of TestsProgram EvaluationReferral and ConsultationTranscription FactorsTruth Disclosure