During a consultation, John remarked: ‘My grandfather and an aunt and uncle died of bowel cancer’. General practitioners are constantly receiving and documenting such information about family members, but how best can it be recorded and interpreted to decide if an individual is at risk for a genetic disorder?
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References
1.
BennettR.L.The practical guide to the genetic family history (1999) New York: Wiley-Liss ISBN 0 471 25154 2
2.
BennettR.L.SteinhausK.A.UhrichS.B.Recommendations for standardized human pedigree nomenclature. American Journal of Human Genetics (1995) 56: p. 745–52
3.
Consent and confidentiality in genetic practice: guidance on genetic testing and sharing genetic information Report of the Joint Committee on Medical Genetics (2005) London: RCP, RCPath, BSHG
4.
QuereshiN.BetheaJ.ModellB.Collecting genetic information in primary care: evaluating a new family history tool. Family Practice (2005) 22: p. 663–9
5.
RichE.C.BurkeW.HeatonC.J.Reconsidering the family history in primary care. Journal of General Internal Medicine (2004) 19: p. 273–80