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  • +91 98288 92000
  • AlIMS Rd, Patrakar Colony, Shastri Nagar, Jodhpur, Rajasthan 342011
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Genetic Testing Jodhpur

Choose the Healthiest Embryo,
Maximize Every Chance

Preimplantation Genetic Testing checks embryos during IVF for selected chromosomal or genetic concerns before transfer.

At Galwa Care Hospital, PGT is considered for recurrent IVF failure, miscarriages, advanced maternal age or known genetic risk.

It helps choose healthier embryos and improve decision-making in advanced fertility treatment.

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Are You Facing These Issues?

Free Consultation
from our Consultants

When Genetic Certainty Changes Everything

Who Should Consider Preimplantation
Genetic Testing?

PGT is recommended in a range of clinical situations where chromosomal or genetic factors may be silently contributing
to IVF failure, pregnancy loss, or the risk of a serious inherited condition in the child.

Recurrent IVF Failure or Repeated Miscarriages

When previous IVF cycles have failed despite good quality embryos, or when a couple has experienced repeated miscarriages without a clear explanation, chromosomal aneuploidy in the embryos is frequently the cause. PGT-A identifies and excludes these abnormal embryos before transfer.

Advanced Maternal Age (35 Years and Above)

The risk of chromosomal errors in embryos increases significantly with maternal age. Women above 35 benefit most from PGT-A, which screens all chromosomes to identify euploid embryos with the highest potential for successful implantation and a healthy live birth.

Known Carrier of a Single Gene Disorder

Couples who carry specific heritable conditions such as Thalassaemia, Cystic Fibrosis, Sickle Cell Disease, Huntington’s Disease, or Spinal Muscular Atrophy require PGT-M to identify and transfer only embryos confirmed to be unaffected by the inherited genetic condition.

Chromosomal Structural Rearrangement in Either Partner

When one or both partners carry a chromosomal translocation, inversion, or deletion identified on karyotyping, PGT-SR identifies embryos with a balanced or normal chromosomal complement, dramatically improving pregnancy success rates and reducing recurrent miscarriage.

Previous Pregnancy or Child with a Chromosomal Condition

Couples who have had a previous pregnancy affected by Down Syndrome or another chromosomal condition, or who have had a child born with a serious genetic disorder, benefit significantly from PGT to reduce the risk of recurrence in subsequent pregnancies.

Unexplained Infertility and Desire to Optimise IVF Outcomes

When no clear cause of infertility has been identified, genetic embryo factors may be silently contributing to failed conception. Couples seeking to maximise IVF success rates by ensuring only genetically healthy embryos are transferred also benefit from PGT-A as part of their treatment strategy.

From Embryo Biopsy to Genetic Certainty

The PGT Procedure Step by Step

Every PGT cycle at Galwa Care Hospital follows a carefully structured, clinically validated process from pre-cycle genetic counselling through to genetically confirmed embryo transfer in collaboration.

Pre-Cycle Genetic Counselling

Medical history, fertility status and goals are reviewed so the safest, most suitable treatment plan can be personalised.

Ovarian Stimulation and Egg Retrieval

Hormonal medicines are given with regular monitoring to support controlled follicle or egg development.

Embryo Culture to Blastocyst Stage

Embryos are cultured and monitored for development, quality and suitability before transfer or freezing.

Trophectoderm Biopsy

Sperm is retrieved directly from the epididymis or testis using the planned surgical technique.

Genetic Laboratory Analysis

The laboratory measures key fertility parameters and prepares clinically useful results for specialist interpretation.

Embryo Vitrification and Awaiting Results

Embryos or reproductive cells are vitrified using rapid freezing and stored in monitored liquid nitrogen tanks.

Embryo Selection and Frozen Embryo Transfer

Suitable options are reviewed carefully so selection remains safe, ethical and aligned with treatment needs.

Genetic Certainty Before Every Transfer

Benefits of Preimplantation Genetic Testing

PGT transforms IVF from a process of hopeful chance into a genetically informed, evidence-based pathway to parenthood, delivering
higher success rates, fewer failed cycles, and the most confident possible embryo selection for every transfer.

Selects Only Chromosomally Healthy Embryos

PGT-A identifies euploid embryos with a normal chromosomal complement, ensuring that only embryos with the highest biological potential for successful implantation and a healthy live birth are selected for transfer.

Significantly Reduces IVF Failure Rates

By excluding chromosomally abnormal embryos that would otherwise fail to implant, PGT dramatically reduces the number of failed transfer cycles, saving couples from the emotional and financial burden of repeated unsuccessful attempts.

Reduces the Risk of Miscarriage

Chromosomal aneuploidy is the leading cause of early miscarriage. PGT-A substantially reduces miscarriage rates by ensuring that only embryos free of the chromosomal errors most responsible for early pregnancy loss are transferred.

Prevents Transmission of Serious Genetic Conditions

PGT-M gives couples who carry heritable single gene disorders the ability to have a child who is unaffected by the condition, providing a pathway to healthy parenthood without the fear of passing on a devastating inherited disease.

Addresses Chromosomal Translocation Carriers

PGT-SR identifies balanced or normal embryos in couples carrying chromosomal structural rearrangements, dramatically improving their chances of a successful pregnancy and reducing the recurrent miscarriage that these rearrangements cause.

Most Valuable for Women Above 35

As the rate of chromosomal errors in embryos rises sharply with maternal age, PGT-A becomes increasingly important and impactful for women above 35, providing the genetic certainty that improves outcomes at exactly the stage where natural embryo selection is least reliable.

Single Embryo Transfer with Confidence

PGT allows confident single embryo transfer by identifying the genetically strongest embryo, reducing multiple pregnancy risk while maintaining high success rates, which is the safest and most clinically optimal approach to IVF.

Eliminates Guesswork from Embryo Selection

Without PGT, embryo selection is based on appearance alone. With PGT, selection is based on confirmed genetic health, transforming embryo assessment from a visual art into an evidence-based, genetically validated clinical science.

Supports Healthier Pregnancies and Babies

Lower chromosomal error rates in transferred embryos are associated with higher quality implantation, reduced early pregnancy complications, and healthier developmental outcomes for the resulting baby throughout pregnancy.

Provides Emotional Certainty and Confidence

For couples who have experienced repeated failure, loss, or the birth of an affected child, PGT provides a level of genetic certainty and emotional reassurance that no other fertility investigation or treatment decision can offer.

Prepare Fully, Proceed with Confidence

PGT Testing — Do's and Don'ts

Following these recommendations before and throughout your PGT IVF cycle will ensure the most accurate genetic testing
results, the most appropriate embryo selection, and the highest possible chance of a successful and healthy pregnancy outcome.

DO'S — What You Should Do

Attend the pre-cycle genetic counselling consultation before the IVF cycle begins.

Share your complete medical, genetic, and family history openly with your fertility specialist.

Complete all pre-cycle karyotyping and carrier screening if recommended before PGT planning.

Allow adequate time for PGT-M protocol development several weeks before the IVF cycle starts.

Follow all ovarian stimulation medication protocols exactly as prescribed throughout the cycle.

Attend every monitoring appointment as follicle tracking is essential for optimal egg retrieval timing.

Allow embryos to develop to the blastocyst stage before biopsy for the most accurate genetic analysis.

Understand that embryos are frozen during the testing period and transfer occurs in a subsequent cycle.

Attend the result consultation promptly to discuss findings and plan the frozen embryo transfer.

Ask your genetic counsellor to explain every result clearly so you fully understand each embryo's status.

DONT'S — What You Should Avoid

Do not skip the pre-cycle genetic counselling as PGT protocol design requires individualised planning.

Avoid starting the IVF cycle before the PGT-M probe has been custom-developed for your specific mutation.

Do not expect PGT to guarantee pregnancy as uterine receptivity and other factors also influence outcomes.

Avoid assuming PGT replaces all prenatal testing as confirmatory testing after transfer is still often recommended.

Do not make embryo transfer decisions based on appearance alone when PGT results are available.

Avoid skipping medication doses during stimulation as consistent hormonal support is critical to cycle success.

Do not request immediate transfer before genetic results are confirmed as this defeats the purpose of PGT.

Avoid interpreting genetic results without your fertility specialist and genetic counsellor present.

Do not lose hope if fewer embryos than expected are genetically normal as this is a common and expected finding.

Avoid delaying PGT if recurrent IVF failure or known genetic carrier status makes it clinically indicated.

Genetic Expertise, Compassionate Fertility Care

The Most Trusted
PGT Programme
in Rajasthan

All three PGT types available including PGT-A, PGT-M, and PGT-SR under one comprehensive programme

Collaboration with accredited genetic laboratories using latest NGS-based testing technology

Dedicated pre-test genetic counselling for every couple before PGT cycle planning begins

Experienced IVF embryologists skilled in blastocyst biopsy with consistent high-quality cell yield

State-of-the-art embryology laboratory ensuring optimal embryo culture to blastocyst stage

Transparent, affordable PGT pricing with clear communication of all costs before the cycle begins

Compassionate, patient-first approach that never loses sight of the emotional weight of this journey

2000+

Eggs Successfully Frozen

98%

Vitrification Survival Rate

15+

Years of Experience

24/7

Support to Call

Advanced Genetic Testing, Transparent Pricing

How Much Does PGT Cost?

The cost of PGT at Galwa Care Hospital depends on the specific type of testing required, the number of embryos biopsied and tested, the laboratory analysis method used, and whether genetic counselling is included. All pricing is communicated clearly and transparently upfront with no hidden charges.

Easy EMI Facility Available

PGT type selected (PGT-A, PGT-M, or PGT-SR)

Number of embryos biopsied and tested

Genetic laboratory analysis fees

Pre-cycle genetic counselling

Embryo vitrification and storage

Frozen embryo transfer cycle

Easy EMI Facility Available

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PGT Questions, Clearly Answered

Frequently AskednQuestions.

Yes. The biopsy involves removing only 5 to 10 cells from a blastocyst that contains over 100 cells, and extensive research confirms no significant impact on the embryo's developmental potential or pregnancy outcomes when performed by skilled embryologists. PGT significantly improves the chances of a successful pregnancy by selecting genetically healthy embryos, but it cannot guarantee a 100% outcome as other factors including uterine receptivity, endometrial preparation, and overall health also play important roles in implantation and pregnancy. PGT gives every transfer the strongest possible genetic foundation, which is the most meaningful improvement any single intervention can make to IVF success rates.

PGT-A screens all 24 chromosome types for numerical abnormalities (aneuploidy) and is recommended for advanced maternal age, recurrent IVF failure, and optimising embryo selection. PGT-M tests for a specific known single gene mutation carried by one or both parents and is recommended for couples at risk of transmitting heritable conditions such as Thalassaemia, Cystic Fibrosis, or Huntington's Disease. PGT-SR identifies embryos with balanced chromosomal material in couples who carry a structural rearrangement such as a translocation, which causes recurrent miscarriage. Your fertility specialist and genetic counsellor at Galwa Care Hospital will recommend the most appropriate type based on your specific history, karyotype, and carrier screening results.

PGT results typically take 1 to 2 weeks to process in the accredited genetics laboratory. During this waiting period, all biopsied embryos are vitrified (frozen) to protect their viability and developmental potential. Once results are confirmed and genetically normal or unaffected embryos are identified, the best candidate is selected for frozen embryo transfer (FET) in a subsequent prepared cycle. This means that the transfer does not occur in the same stimulation cycle as the egg retrieval, but in a separate dedicated FET cycle where the uterine lining is specifically prepared for the best possible implantation conditions.

Yes, PGT-A is strongly recommended for women 35 and above as the risk of chromosomal aneuploidy in embryos increases significantly with maternal age, and selecting euploid embryos through PGT-A substantially improves IVF success rates and reduces miscarriage risk in this age group. Regarding previously frozen embryos, PGT generally requires a fresh biopsy from a blastocyst-stage embryo. Previously frozen embryos can technically be thawed, biopsied, and re-frozen, but this adds additional handling steps and is discussed on a case-by-case basis by our fertility team at Galwa Care Hospital based on the quality and developmental stage of the stored embryos.

PGT reduces but does not eliminate the need for prenatal testing. Many doctors still recommend confirmatory prenatal investigations such as NIPT or amniocentesis after a PGT-screened pregnancy for additional reassurance, as PGT tests only the specific genetic parameters for which it was designed. PGT can detect chromosomal aneuploidy across all chromosomes, hundreds of single gene disorders, and structural rearrangements, but it cannot screen for every possible genetic condition. Pre-test genetic counselling at Galwa Care Hospital sets realistic expectations, explains precisely what the selected PGT type will and will not detect, and helps every couple approach the process with the most complete and honest understanding of its capabilities and its limitations.

Transparent, affordable PGT pricing with clear communication of all costs before the cycle begins

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