TreatmentsPgt

    Preimplantation Genetic Testing in HSR Layout, Bangalore

    Preimplantation Genetic Testing (PGT) is a type of genetic screening used during assisted reproductive technology (ART) treatments such as in vitro fertilization (IVF). It is performed on embryos before they are implanted into the uterus to detect any genetic or chromosomal abnormalities.

    Types of PGT

    There are two main types of PGT: PGT-A (for aneuploidy) and PGT-M (for monogenic/single gene disorders). PGT-A screens for chromosomes that are missing or have extra copies, while PGT-M screens for specific genetic disorders such as cystic fibrosis or sickle cell anemia.

    Process

    The process of PGT involves removing one or two cells from an eight-cell embryo, which is then tested for any genetic abnormalities. The results of the test can then be used to determine the best embryos to transfer for maximum chances of a successful pregnancy.

    Benefits

    PGT can increase the chances of having a healthy baby, reduce the risk of miscarriage, and minimize the chance of passing on genetic disorders to the child. It is particularly useful for older women or couples with a history of genetic disorders.

    Summary

    Overall, PGT is a valuable tool in the field of reproductive medicine and can greatly enhance the success of ART treatments. However, it is important to discuss the potential benefits and risks of PGT with a fertility specialist before making a decision.

    FAQ's on PGT Treatment

    Preimplantation Genetic Testing (PGT) is a type of genetic screening performed during assisted reproductive technology (ART) treatments such as in vitro fertilization (IVF). It is used to detect any genetic or chromosomal abnormalities in embryos before they are implanted into the uterus.

    PGT is recommended for couples who have a history of genetic disorders, older women, or those who have experienced recurrent miscarriages. It can increase the chances of having a healthy baby, reduce the risk of miscarriage, and minimize the chance of passing on genetic disorders to the child.

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