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Preimplantation Genetic Screening

PGS screens the embryo for normal chromosome number. There can be extra (trisomy) or missing (monosomy) chromosomes. Both conditions are a problem. Biopsy at the cleavage stage is done on day 3 of embryo development. The main indications for the use of PGS in IVF treatments include advanced maternal age, repeated implantation failure, and recurrent pregnancy loss. The aim of PGS is to prevent reccurent miscarriages and to avoid having a child affected with the most common aneuploidy disorders – Down Syndrome (trisomy 21), Edwards Syndrome (trisomy 18), Patau Syndrome (trisomy 13), Turner syndrome (monosomy X), and Klinefelter syndrome (Gonosomal trisomy XXY). These trisomies originate from meiotic errors that may arise during the formation of gametes, especially in women.

1,000.00 1000.0 USD

25,000.00 ₹

SKU: RPKRT2


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