
There are several reports of an earlier age of diagnosis in successive generations amongst BRCA1/2 mutation carrier families, which may indicate an anticipation phenomenon among hereditary breast cancer (BC) patients. The study aims to determine this anticipation by evaluating trends in age at diagnosis and phenotype of BC across two successive generation pairs of BRCA1/2 mutation carriers/non‐carriers with BC. The present study also observed a downshift at the age of diagnosis in non‐carrier pairs, emphasizing that other factors (environmental, lifestyle or social) may influence the generation at diagnosis.
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