The recent identification of the BRCA1 and BRCA2 genes has improved our und
erstanding of the association between breast and ovarian cancers in certain
families. Carriers of predisposing germline mutations must decide on diffe
rent options for management, including close follow-up or prophylactic surg
ery. Further studies are needed to elucidate the optimal management of thes
e patients and to identify the factors that modify their risk for developin
g breast cancer. Finally, we must work to prevent any form of discriminatio
n against those who, following, genetic testing, are found to be at increas
ed risk for breast cancer.