Prenatal genetic testing and counseling
Prenatal genetic testing gives expecting parents information about whether their fetus has genetic abnormalities, including genetic disorders (such as Down syndrome and other aneuploidies, deletions, and duplications) or single-gene disorders (such as sickle cell disease, cystic fibrosis, and Tay-Sachs disease). Our imaging team offers patients a full range of prenatal genetic screening and testing, including chorionic villus sampling (CVS) and amniocentesis to help them along their journey. If needed, a patient’s ob-gyn can provide a referral for genetic counseling.
Hereditary cancer risk assessment
We offer genetic risk assessment and counseling for individuals with personal and family histories of breast and gynecologic cancers of the ovaries and uterus, hereditary colon cancer and other cancer predisposition syndromes. Our patients receive comprehensive information about the recommended cancer genetic testing approach with personalized counseling to support decision-making and next steps. We work closely with our patient’s providers to integrate the test results into the patient’s managed care plan, which may include regular screenings and follow-up care.