What is PGD & NGS?
Preimplantation Genetic Diagnosis (PGD):
PGD is a specialized testing method used to identify specific inherited genetic conditions in embryos, such as cystic fibrosis, Tay-Sachs, or sickle cell anemia. This ensures that only embryos free of these conditions are selected for transfer during IVF.
Next-Generation Sequencing (NGS):
NGS is a more comprehensive technique that analyzes all chromosomes for abnormalities, such as aneuploidies (extra or missing chromosomes). This method significantly improves embryo selection and increases the chances of successful implantation.
The PGD & NGS Process:
1. Fertilization and Embryo Development:
During IVF, embryos are created and allowed to develop to the blastocyst stage in our state-of-the-art laboratory.
3. Genetic Testing:
The extracted cells are analyzed using PGD or NGS to detect genetic or chromosomal abnormalities.
2. Biopsy and Analysis:
A small number of cells are carefully extracted from the embryo for testing, without harming its development.
4. Embryo Selection:
Only the healthiest embryos are selected for transfer, optimizing the chances of a successful pregnancy and a healthy baby.
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