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Explore Preimplantation Genetic Screening Clinics

Preimplantation genetic screening (PGS), also known as preimplantation genetic testing for aneuploidy (PGT-A), is a procedure used in reproductive medicine to screen embryos for chromosomal abnormalities before they are transferred to the uterus during in vitro fertilization (IVF). By enhancing the chances of a successful pregnancy, PGS offers hope and reassurance to families on their journey to parenthood.

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FAQ ABOUT Explore Preimplantation Genetic Screening Clinics

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  • What genetic conditions can PGS detect?

    PGS or PGT-A screens for chromosomal aneuploidies like Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13). It does not test for specific genetic diseases but evaluates chromosomal normalcy to support a healthy pregnancy.

  • How does PGS increase the chances of a successful IVF cycle?

    PGS improves IVF success by selecting euploid embryos, reducing miscarriage risk, and increasing chances of a full-term pregnancy.

  • Is PGS recommended for all couples undergoing IVF?

    PGS is recommended for women over 35, couples with recurrent miscarriages, failed IVF cycles, or a history of chromosomal anomalies. The decision should be personalized based on age, fertility history, and risk factors.

  • How long does the PGS process take?

    PGS adds time to the IVF cycle, as embryo analysis takes 1-2 weeks. Embryos may need to be frozen until results are ready for a later transfer.

  • Can PGS guarantee the birth of a healthy child?

    PGS reduces the risk of chromosomal anomalies but cannot guarantee a healthy child. It doesn't screen for all genetic or congenital conditions, though it improves IVF outcomes.

Explore Preimplantation Genetic Screening Clinics