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HomeTestPgt A 9 Embryos Test

PGT-A (9 Embryos) Test: Booking, Price, and Results

About PGT-A (9 Embryos) Test: Booking, Price, and Results

FieldValue
Also Known AsPGS (Preimplantation Genetic Screening), Preimplantation Genetic Testing for Aneuploidy, Embryo Chromosome Screening
Sample TypeTrophectoderm biopsy (cells from the outer layer of a blastocyst-stage embryo)
Fasting RequiredNot applicable — the test is performed on embryo cells, not on the patient
Report Time18 days
Recommended ForCouples undergoing IVF, particularly women aged 35 and above, those with recurrent miscarriages, recurrent implantation failure, or a prior chromosomally abnormal pregnancy
PriceStarting at ₹90,000

What is a PGT-A (9 Embryos) Test?

The PGT-A test (Preimplantation Genetic Testing for Aneuploidy) is a specialised genetic screening performed during an IVF cycle. It examines embryos for chromosomal abnormalities before they are transferred to the uterus. The PGT-A (9 embryos) test covers screening of up to nine blastocyst-stage embryos in a single panel. It is also known as Preimplantation Genetic Screening (PGS) or Embryo Chromosome Screening.

What Does a PGT-A (9 Embryos) Test Measure?

The PGT-A test uses Next-Generation Sequencing (NGS) technology to analyse all 23 chromosome pairs in each embryo. Here is what the test evaluates:

ParameterWhat it Checks
Euploidy StatusWhether the embryo has the correct number of 46 chromosomes (23 pairs)
Aneuploidy DetectionWhether any chromosomes are missing or present in extra copies
MosaicismWhether the embryo contains a mix of chromosomally normal and abnormal cells
Segmental AneuploidyWhether portions of chromosomes (rather than whole chromosomes) are missing or duplicated

Why is a PGT-A (9 Embryos) Test Done?

The PGT-A test is recommended for couples undergoing IVF who want to improve the chances of a successful embryo transfer. A doctor may suggest it based on specific clinical circumstances.

Common Symptoms That May Require This Test

While PGT-A is not triggered by symptoms in the traditional sense, the following situations commonly lead a fertility specialist to recommend it:

  • Advanced maternal age (35 years or older at the time of egg retrieval)
  • A history of two or more unexplained miscarriages
  • Repeated IVF cycles that have not resulted in a successful pregnancy
  • A previous pregnancy or child with a chromosomal condition
  • Known chromosomal translocations or rearrangements in either partner
  • Severe male factor infertility
  • A desire to improve embryo selection for transfer

Conditions This Test Can Help Detect

The PGT-A test can identify embryos affected by the following:

  • Trisomy 21 (Down syndrome)
  • Trisomy 18 (Edwards syndrome)
  • Trisomy 13 (Patau syndrome)
  • Other whole-chromosome gains or losses across all 23 pairs
  • Segmental chromosomal imbalances

How to Prepare and What to Expect

Because this test is performed on embryo cells rather than a patient's blood or urine sample, preparation is different from a standard diagnostic test. Below is everything you need to know before proceeding.

Do You Need to Fast?

No fasting is required. The PGT-A test procedure is carried out on embryo biopsy cells in the laboratory. There is no dietary restriction for the patient.

Practical Tips Before Your Test

Here are some practical steps to take before your embryos are tested:

  • Complete a full IVF cycle, including ovarian stimulation and egg retrieval, before PGT-A can be arranged
  • Attend genetic counselling before the test to understand what the results can and cannot tell you
  • Bring a detailed clinical history, including your symptoms, previous test results, and family history, as this is required for the test
  • Ensure you carry the duly completed Test Request Form (TRF), biopsy worksheet, and signed consent form, as these are mandatory for processing
  • Be prepared for your embryos to be frozen (vitrified) immediately after biopsy, while results are awaited
  • Confirm that your IVF centre has trained embryologists and the necessary equipment for trophectoderm biopsy

Step-by-Step Procedure

The PGT-A test procedure involves several stages carried out by your IVF team and the genetics laboratory:

  1. IVF cycle completion: Eggs are retrieved, fertilised in the laboratory, and cultured for five to six days until they reach the blastocyst stage.
  2. Embryo biopsy: A trained embryologist uses a laser to open a small gap in the embryo's outer shell and removes five to eight cells from the trophectoderm (the outer layer that would form the placenta). The inner cell mass, which develops into the baby, is left undisturbed.
  3. Embryo freezing: All biopsied embryos are immediately vitrified (frozen) and stored safely while testing is underway.
  4. Sample dispatch: Biopsy cells are placed in the PGT Collection Kit and transported on dry ice to the Lupin Diagnostics genetics laboratory.
  5. NGS analysis: The laboratory uses Next-Generation Sequencing to examine all 23 chromosome pairs in each embryo sample.
  6. Results and next steps: Once results are ready, your fertility specialist reviews the findings and identifies euploid embryos suitable for frozen embryo transfer.

Factors That Can Affect Accuracy

The following factors may influence the reliability of PGT-A test results:

  • The skill and experience of the embryologist performing the biopsy
  • The developmental stage and quality of each embryo at the time of biopsy
  • Natural embryonic mosaicism (some embryos contain a mix of normal and abnormal cells)
  • Laboratory sequencing conditions and analytical methods
  • The fact that biopsy samples come only from the trophectoderm, which may not always fully represent the inner cell mass

Understanding Your PGT-A (9 Embryos) Test Results

Results from the PGT-A test are reported for each embryo individually. Your fertility specialist and genetic counsellor will review each result and guide your transfer decisions. The table below outlines the possible result categories:

Result CategoryMeaningClinical Significance
EuploidNormal — 46 chromosomes present (23 pairs)Suitable for embryo transfer; highest likelihood of successful implantation
AneuploidAbnormal — chromosomes missing or in excessNot recommended for transfer; associated with higher risk of implantation failure or miscarriage
MosaicMixed — embryo contains both normal and abnormal cellsTransfer decision made on a case-by-case basis with specialist guidance
InconclusiveUnable to determine chromosomal statusMay require re-biopsy of the embryo

Disclaimer: These ranges are general guidelines. Your doctor will interpret your results based on your age, health history, and other factors. Always consult a qualified healthcare professional for personalised medical advice.

Results During Special Conditions

Embryonic mosaicism is an important factor to be aware of when reviewing results. Some embryos naturally contain a proportion of chromosomally normal and abnormal cells. This can affect what the biopsy sample reflects, since only trophectoderm cells are tested. Mosaic embryos may still result in a healthy birth, but the transfer decision requires careful discussion with a genetic counsellor and fertility specialist.

Research indicates that aneuploidy rates increase with maternal age, rising from approximately 28% in women below 30 years to around 68% in women over 40. This means older patients are more likely to have aneuploid embryos identified through testing.

How to Maintain Healthy Levels

While chromosomal status cannot be changed, there are general steps that support a positive IVF outcome:

  • Discuss all results, including mosaic findings, thoroughly with your fertility specialist and genetic counsellor before deciding on embryo transfer
  • Continue with standard prenatal screening after a successful transfer, as PGT-A does not replace routine pregnancy testing
  • Maintain general reproductive health through balanced nutrition, adequate rest, and regular communication with your healthcare team

Lupin Diagnostics PGT-A (9 Embryos) Test Price

The PGT-A test cost at Lupin Diagnostics starts at ₹90,000 for a panel of nine embryos. This test requires a visit to a Lupin Diagnostics centre; home collection is not available for this test.

CityApproximate Price (₹)
BHOPAL90000
CHENNAI90000
HYDERABAD90000
KOLKATA90000
NAVI MUMBAI90000
PUNE90000

Disclaimer: Prices are indicative and may vary by location. Please confirm the current price at the time of booking.

How to Book

Here is how to book your PGT-A test online with Lupin Diagnostics:

  1. Select the PGT-A (9 Embryos) test on the Lupin Diagnostics website.
  2. Choose your city and preferred centre location.
  3. Visit the centre at your scheduled time, bringing your completed TRF, biopsy worksheet, signed consent form, and clinical history.
  4. Receive your report via email or WhatsApp within the stipulated turnaround time.

Frequently Asked Questions

The PGT-A test screens embryos for chromosomal number abnormalities (too many or too few chromosomes). It does not test for specific inherited diseases or single-gene disorders. PGT-M is used for couples with a known inherited genetic condition, while PGT-SR screens for structural chromosomal rearrangements such as translocations.

The PGT-A test is typically recommended for women aged 35 and above undergoing IVF, those with recurrent miscarriages, couples with repeated failed IVF transfers, and those with a previous pregnancy affected by a chromosomal condition. A fertility specialist can advise whether it is appropriate for your situation.

The biopsy removes cells only from the outer layer of the embryo (the trophectoderm), leaving the inner cell mass undisturbed. Studies to date have reported reassuring neonatal outcomes following trophectoderm biopsy. Your IVF team will explain the procedure and any associated considerations before you consent.

At Lupin Diagnostics, the report delivery time for the PGT-A (9 embryos) test is 18 days from the date the laboratory receives the biopsy sample. Your embryos remain safely frozen during this period.

If no euploid embryos are identified from the current cycle, your fertility specialist may recommend an additional IVF retrieval cycle to produce further embryos for testing. The right next step depends on your individual clinical situation and should be discussed in detail with your doctor.

Yes, there are documented cases of healthy births following the transfer of mosaic embryos. However, mosaic embryos may carry a lower chance of successful implantation. Any decision to transfer a mosaic embryo should be made only after thorough counselling with a genetic specialist and your fertility doctor.

No. The PGT-A test improves embryo selection by identifying chromosomally normal embryos, which can reduce the risk of miscarriage and failed transfers. However, it does not guarantee pregnancy. Standard prenatal screening is still recommended after conception, even when a euploid embryo has been transferred.

PGT-A (9 Embryos) Test: Booking, Price, and Results

Price
90,000.00
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