From What I Understand
THOSE WHO ARE TRIPLE NEGATIVE (her2-er-pr-) ARE MUCH MORE LIKELY TO HAVE THE GENETIC DEFECTS THEY ARE TESTING FOR with BRCA1/2 (please correct me if I am wrong on this) than her2+ patients
They can also look for wrong numbers of parts of chromosomes and shortened chromosomes but that I understand is not what they are doing typically when someone goes for simple genetic testing for breast cancer.
I was also informed that those with a family history of women getting breast cancer LATE in their lives were unlikely to habe the BRCA1/2 defect.
Can anyone else chime in?
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