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- W2004581049 abstract "Funding: The development of this material was supported in part through funding from the Genetics in Primary Care (GPC): A Faculty Development Initiative. The GPC is a contract (# 240-98-0020) funded by the Maternal and Child Health Bureau and Bureau of Health Professions, Health Resources and Services Administration, with co-funding from the National Human Genome Research Institute, National Institutes of Health, and the Agency for Healthcare Research and Quality.Your patient, a 36-year-old woman, recently learned that her former college roommate was diagnosed with breast cancer. She wants to know if she should have the genetic test her friend mentioned to assess her risk. Her only family history is that her mother has breast cancer at age 72. She mentions that her roommate did not have a family history of breast cancer, “except on her father's side, and that doesn't count.” Table 1Nongenetic contributors to breast cancer risk Menarche before age 12 yearsMenopause after age 55 yearsFirst live birth after age 30 yearsNulliparityPrevious breast biopsiesAtypical hyperplasia diagnosed by breast biopsyObesityAlcohol useHormone replacement therapyExcessive radiation exposureView it in a separate window" @default.
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- W2004581049 date "2001-09-01" @default.
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- W2004581049 title "Why should primary care physicians know about breast cancer genetics?" @default.
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- W2004581049 doi "https://doi.org/10.1136/ewjm.175.3.168" @default.
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