Pre-Implantation Genetic Screening (PGS)
- How it Works
- Suitable For
- Process
- Cost
- Results
- Success Rate
- FAQs
Reproductive healthcare has evolved significantly with advancements in modern science, including Assisted Reproductive Technology (ART). One such advancement is Pre-implantation Genetic Testing (PGT), which helps identify potential chromosomal anomalies or genetic disorders at the embryo development stage. PGT treatment improves pregnancy outcomes with minimal risks. This article discusses PGT treatment in detail, its benefits, procedure, and cost.
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What Is Pre-Implantation Genetic Testing & How Does it Work?
PGT is a method that identifies any genetic defects in an embryo created through an in vitro fertilization (IVF) procedure. Pre-implantation Genetic Testing (PGT) is done before the embryo is transferred into the uterus, to ensure a healthy and successful pregnancy. This method significantly reduces the risk of miscarriages and genetic disorders in the babies born through the IVF procedure.
Step By Step PGT-A Treatment Process
Here is a step-by-step process of an PGT-A treatment
Pre-Care
Treatment
Post-Care
How Much Does Pre-Implant Genetic Testing Cost In India?
The cost of the Pre-implantation Genetic Testing procedure can range from INR 5000 to INR 27000. The cost of the treatment depends on several factors, such as the doctor’s experience, the clinic’s reputation, the geographical location and the couple’s reproductive health status.
Disclaimer: The treatment costs mentioned above are approximate and can vary. Additional charges for medications, diagnostic tests, and extra procedures may apply. Avail a free consultation with us to get a personalised treatment plan and an accurate cost estimate.
Benefits Of PGT Treatment
The treatment offers the following benefits:
Hope for parenthood
IVF is an advanced treatment that provides a ray of hope to couples struggling to achieve pregnancy for years.
Chances of having a healthy baby
The procedure minimises the risk of passing any genetic disorder or chromosomal abnormalities to the baby as the procedure involves transferring the healthiest embryos into a woman's body.
