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For many couples in Bangladesh facing fertility challenges, the journey towards a healthy pregnancy can be filled with uncertainty. Questions about embryo health and the potential for genetic conditions are significant concerns. Exploring advanced testing options like PGT-A/PGT-M becomes essential to address these anxieties and improve outcomes.
Patients often seek medical care beyond their home country when specialized expertise and state-of-the-art technology are desired. India stands out as a leading destination, offering comprehensive PGT-A/PGT-M services across its major cities. This availability provides a wider choice for those seeking genetic insights into their embryos.
India's medical infrastructure is renowned for its high standards in fertility treatments, supported by advanced hospitals and highly skilled specialists. The country boasts numerous accredited centers equipped with cutting-edge laboratories, ensuring precision and reliability in genetic testing procedures. This robust system builds confidence for international patients.
India provides comprehensive PGT-A/PGT-M genetic testing solutions for international patients.
Preimplantation Genetic Testing for Aneuploidy (PGT-A) and Preimplantation Genetic Testing for Monogenic Disorders (PGT-M) are advanced diagnostic tools used in conjunction with In Vitro Fertilization (IVF). PGT-A screens embryos for chromosomal abnormalities like extra or missing chromosomes, aiming to identify embryos with the correct number of chromosomes for transfer. PGT-M, on the other hand, is specifically designed to detect single gene disorders in embryos when one or both parents are known carriers of a specific genetic condition, preventing the inheritance of such diseases. Both tests involve analyzing a small biopsy from the embryo to provide crucial genetic information before implantation.
There are primary categories of preimplantation genetic testing:
The PGT-A/PGT-M procedure involves several precise steps, ensuring careful analysis of embryos within an IVF cycle.
The process begins with a standard IVF cycle. This includes ovarian stimulation, egg retrieval, and fertilization with sperm in the laboratory to create embryos. The embryos are then cultured for five to six days until they reach the blastocyst stage.
Once embryos reach the blastocyst stage, a highly skilled embryologist performs a delicate biopsy. This involves carefully removing a few cells (trophectoderm cells) from the outer layer of the blastocyst, which will later form the placenta. The inner cell mass, which develops into the fetus, is not touched.
The biopsied cells are sent to a specialized genetic laboratory for analysis. For PGT-A, the cells are screened for chromosomal aneuploidies. For PGT-M, they are tested for the specific single gene mutation identified in the parents. This analysis typically takes several days to complete.
After the biopsy, the embryos are cryopreserved (frozen) while awaiting the genetic test results. Once results are available, only chromosomally normal and genetically healthy embryos (free from the specific disorder) are selected for transfer. The chosen embryo is thawed and transferred into the woman's uterus during a subsequent cycle.
Following an embryo transfer after PGT-A/PGT-M, patients are advised to rest and avoid strenuous activities for a day or two. There are usually no significant physical recovery demands beyond the standard IVF transfer experience. Patients often experience a waiting period of about two weeks before a pregnancy test can confirm success. Emotional support during this time is crucial. Follow-up appointments will include monitoring for early pregnancy and continued guidance from the fertility team.
The success rates of PGT-A/PGT-M are generally high for identifying chromosomal abnormalities and specific genetic disorders. While PGT-A improves implantation and live birth rates by reducing miscarriages, it does not guarantee a pregnancy. Success varies based on factors such as the woman's age, number of embryos available, overall embryo quality, and the specific genetic condition being tested. Long-term expectations involve a higher likelihood of a healthy, term pregnancy compared to IVF without PGT.
The cost of PGT-A/PGT-M testing in India varies significantly based on several factors. These include the reputation and facilities of the fertility clinic, the experience of the genetic specialists, the type of PGT performed (A or M), the number of embryos biopsied and tested, and any additional genetic counseling or advanced laboratory techniques required.
Typically, the cost for PGT-A/PGT-M (per cycle for biopsy and testing of a batch of embryos) in India can range from INR 1,00,000 to INR 2,70,000, excluding the IVF cycle costs.
| City | Estimated Cost (INR) |
|---|---|
| Delhi | 1,20,000 - 2,50,000 |
| Mumbai | 1,30,000 - 2,70,000 |
| Chennai | 1,10,000 - 2,30,000 |
| Bengaluru | 1,25,000 - 2,60,000 |
| Hyderabad | 1,15,000 - 2,40,000 |
| Kolkata | 1,00,000 - 2,20,000 |
| Ahmedabad | 95,000 - 2,10,000 |
| Country | Estimated Cost (INR) |
|---|---|
| India | 1,00,000 - 2,70,000 |
| USA | 5,00,000 - 10,00,000+ |
| UK | 4,00,000 - 8,00,000+ |
| Australia | 4,50,000 - 9,00,000+ |
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