PGS Testing 3rd Day Biopsy - 8 Embryos Test, Price, Normal Range - Sprint Diagnostics Hyderabad

Patient Preparing : None

₹ 10800


Preimplantation Genetic Screening (PGS) is an advanced technique that allows for the screening of chromosomal abnormalities in embryos during an In-Vitro Fertilization (IVF) cycle. The process involves the removal of a few cells from each embryo on the third day post-fertilization, when the embryo is comprised of about 6-8 cells. PGS testing offers crucial insights into the genetic health of an embryo, improving the chances of a successful pregnancy and a healthy baby.

The procedure is especially recommended for couples with a history of recurrent miscarriages, multiple failed IVF cycles, advanced maternal age, severe male factor infertility, or a family history of chromosomal disorders. By ensuring the transfer of chromosomally normal embryos, PGS can significantly enhance the probability of a successful IVF outcome.

Test Name PGS Testing 3rd Day Biopsy - 8 Embryos
Sample Type Embryos
Preparations Required None
Report Time 24 hours
Price in Hyderabad ₹ 10800

What does PGS testing involve?

PGS testing involves the removal of a few cells from each embryo on the third day of development, at a stage when the embryo consists of about 6-8 cells. These cells are then analyzed for chromosomal abnormalities, while the embryo is preserved and, if healthy, can later be transferred into the uterus.

How does PGS testing help in improving pregnancy outcomes?

PGS testing improves pregnancy outcomes by ensuring that only chromosomally normal embryos are transferred into the uterus. This reduces the risk of miscarriages and increases the chances of a successful pregnancy and a healthy baby.

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Who is PGS testing recommended for?

PGS testing is recommended for couples with a history of recurrent miscarriages, failed IVF cycles, those with advanced maternal age, severe male factor infertility, or a family history of chromosomal disorders.

Are there any risks associated with PGS testing?

The process of PGS testing involves removing a few cells from the embryo. This is a delicate procedure, but when performed by experienced professionals, the risks to the embryo are minimal.

Does PGS testing guarantee a successful pregnancy and a healthy baby?

While PGS testing significantly improves the chances of a successful pregnancy and a healthy baby by ensuring the transfer of chromosomally normal embryos, it does not guarantee it. Other factors such as the woman's overall health, uterine conditions, and unforeseen complications can affect pregnancy outcomes.

How accurate is PGS testing?

PGS testing is a highly accurate technique for detecting chromosomal abnormalities in embryos. However, it's important to note that the test does not detect single gene disorders unless they involve a whole chromosome or a large part of it.

Can PGS testing determine the sex of the embryos?

Yes, PGS testing can determine the sex of the embryos as it involves the analysis of all 23 pairs of chromosomes, which includes the X and Y sex chromosomes.

What happens if all my embryos have chromosomal abnormalities?

If all your embryos are found to have chromosomal abnormalities, your doctor will discuss the next steps with you. These might involve another IVF cycle, considering the use of donor eggs or sperm, or exploring other fertility treatment options.

How long does it take to get the results of PGS testing?

The results of PGS testing are typically available within 7-10 days. Your doctor will then discuss the results with you and plan the next steps accordingly.

What happens to the embryos after the PGS testing?

After PGS testing, chromosomally normal embryos can be transferred into the uterus in a subsequent cycle. The remaining healthy embryos can be frozen for future use.

Can I do PGS testing if I'm using donor eggs or sperm?

Yes, PGS testing can be performed on embryos created with either donor eggs or sperm. The test can provide valuable information about the chromosomal health of these embryos.

Can PGS detect all genetic diseases?

PGS can detect chromosomal abnormalities, which are a cause of many genetic diseases. However, it cannot detect single gene disorders unless they involve a whole chromosome or a large part of it.

Can I choose the sex of my baby using PGS?

While PGS can determine the sex of the embryos, the use of this information for sex selection is subject to ethical considerations and legal regulations, which vary from place to place.

Does PGS increase the success rate of IVF?

Yes, by ensuring the transfer of chromosomally normal embryos, PGS can significantly increase the success rate of IVF.

Is PGS testing painful?

No, PGS testing is not painful for the patient as the biopsy is performed on the embryos outside of the body.

In conclusion, PGS testing is a revolutionary procedure that helps in increasing the chances of a successful pregnancy in an IVF cycle, reducing the risk of miscarriage, and ensuring the birth of a chromosomally healthy baby. As with any procedure, it's important to discuss with your healthcare provider to understand the benefits and any potential risks.

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