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dc.contributor.authorKerr, Bronwyn
dc.contributor.authorFoulkes, William D
dc.contributor.authorCade, D
dc.contributor.authorHadfield, L
dc.contributor.authorHopwood, Penelope
dc.contributor.authorSerruya, Corinne
dc.contributor.authorHoare, E
dc.contributor.authorNarod, Steven A
dc.contributor.authorEvans, D Gareth R
dc.date.accessioned2010-02-12T10:59:43Z
dc.date.available2010-02-12T10:59:43Z
dc.date.issued1998-08
dc.identifier.citationFalse family history of breast cancer in the family cancer clinic. 1998, 24 (4):275-9 Eur J Surg Oncolen
dc.identifier.issn0748-7983
dc.identifier.pmid9724992
dc.identifier.doi10.1016/S0748-7983(98)80005-X
dc.identifier.urihttp://hdl.handle.net/10541/91917
dc.description.abstractAIMS: Awareness of hereditary breast and ovarian cancer in both the general public and the medical profession is increasing. Individuals who may be at risk on the basis of a family history are requesting risk determination and appropriate management in a variety of settings. Risk determination relies largely on pedigree analysis and epidemiological data. METHODS: We describe five individuals presenting in the family cancer or genetic counselling clinic where a factitious family or personal history led to erroneous risk estimation. Common factors in these families are a history of benign breast disease, poor communication within families, long survival with early onset or bilateral disease, a lack of detailed knowledge of the illness and treatment in close relatives and inconsistencies in the history in repeated consultations.
dc.language.isoenen
dc.subjectBreast Canceren
dc.subject.meshAdult
dc.subject.meshBreast Neoplasms
dc.subject.meshFamily Relations
dc.subject.meshFemale
dc.subject.meshGenetic Counseling
dc.subject.meshGreat Britain
dc.subject.meshHumans
dc.subject.meshPedigree
dc.subject.meshRisk
dc.subject.meshUnited States
dc.titleFalse family history of breast cancer in the family cancer clinic.en
dc.typeArticleen
dc.contributor.departmentDepartment of Medical Genetics, St Mary's Hospital, Manchester.en
dc.identifier.journalEuropean Journal of Surgical Oncologyen
html.description.abstractAIMS: Awareness of hereditary breast and ovarian cancer in both the general public and the medical profession is increasing. Individuals who may be at risk on the basis of a family history are requesting risk determination and appropriate management in a variety of settings. Risk determination relies largely on pedigree analysis and epidemiological data. METHODS: We describe five individuals presenting in the family cancer or genetic counselling clinic where a factitious family or personal history led to erroneous risk estimation. Common factors in these families are a history of benign breast disease, poor communication within families, long survival with early onset or bilateral disease, a lack of detailed knowledge of the illness and treatment in close relatives and inconsistencies in the history in repeated consultations.


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