Genetics with IVF
During an IVF–ICSI cycle, after egg retrieval (OPU) and fertilization via ICSI, a small number of cells are carefully taken from each embryo for analysis in the Genetics Laboratory. Embryo transfer is performed once the genetic test results are available. Genetic testing during IVF provides detailed insights into the health of each embryo before transfer, without affecting the overall duration of treatment.
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The Following Genetic Tests May Be Completed During An IVF Cycle:
Family Balancing through Gender Selection: Screen your embryos to identify the gender and check for chromosomal abnormality such as Down Syndrome.
Comprehensive Chromosomal Screening (CCS) for Chromosomal Abnormalities: Screen all 24 chromosomes for gender as well as any chromosomal abnormalities caused by missing or additional chromosomes. Chromosomal abnormalities include Trisomy 13 (Down syndrome), Trisomy 18 (Edward’s syndrome) and Trisomy 21 (Patau’s syndrome). Chromosomal abnormalities are the leading cause of miscarriage.
HLA Matching Curing a Family Member: Cure a family member suffering from a hereditary disease curable by bone marrow transplant by identifying an HLA Match during IVF.