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PGD/PGS

Pre Implantation Genetic Diagnosis and Screening to increase your chances of carrying a successful pregnancy and a healthy baby

Preimplantation genetic diagnosis (PGD) for single gene disorders is a powerful genetic test to screen embryos that are at risk ofdeveloping a serious genetic disease.

Preimplantation genetic screening (PGS) is used to identify embryos which are free of any chromosomal abnormalities. PGS offers comprehensive analysis of 24 chromosomes including X & Y to detect any chromosomal aneuploidies that might be present in the embryo.

Uniqueness of iGenetic

At iGenetic, PGD is done to screen for most common genetic disorders which are Downs' syndrome, alpha and beta Thalessemia, Sickle cell anemia, Muscular dystrophy, G6PD and Cystic fibrosis.

Test

PGD and PGS

Method Sample required
FISH, Molecular Genetics, and Next Generation Sequencing 3rd day Blastomere biopsy/ 5th day Trophoblast biopsy
Method FISH, Molecular Genetics, and Next Generation Sequencing
Sample required 3rd day Blastomere biopsy/ 5th day Trophoblast biopsy
How to Order:
Prior information needed to order this test.

Please contact us by phone or email to schedule a test.

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