Preimplantation Genetic Testing (PGT)

Preimplantation Genetic Testing

Preimplantation Genetic Testing, commonly known as PGT, is one of the most advanced technologies used in modern fertility care. It allows embryos created through IVF to be screened for genetic or chromosomal abnormalities before they are transferred into the uterus. For many individuals and couples, PGT offers peace of mind, improved pregnancy rates, and a stronger chance of welcoming a healthy baby. This testing is especially valuable for those with a history of genetic disorders, repeated miscarriages, advanced maternal age, or unexplained IVF failures.

Leading global organisations such as the American Society for Reproductive Medicine (ASRM) and the World Health Organization (WHO) recognise PGT as an important step for identifying conditions that may affect embryo health and pregnancy outcomes. At our IVF Fertility Centre, we offer PGT with strict laboratory standards, precise genetic analysis, and compassionate counselling to help you understand the results clearly and confidently.

Our PGT Services

PGT-A for Chromosomal Screening

PGT-A, or Preimplantation Genetic Testing for Aneuploidy, screens embryos for chromosomal abnormalities such as missing or extra chromosomes. Conditions like Down syndrome, Turner syndrome, and other chromosomal disorders can be identified through this testing. PGT-A helps select embryos with the correct number of chromosomes, improving the chances of implantation and reducing the risk of miscarriage. This service is especially beneficial for women over 35 and couples with recurring IVF failures.

PGT-M for Single Gene Disorders

PGT-M is used when one or both partners carry a known genetic disorder, such as thalassemia, sickle cell disease, cystic fibrosis, or muscular dystrophy. This test examines embryos for the specific gene mutation before transfer. PGT-M provides a safe way to prevent passing inherited conditions to future generations. Couples receive full counselling to understand the genetic pathway and make informed choices regarding embryo selection.

PGT-SR for Structural Chromosomal Rearrangements

PGT-SR is designed for individuals or couples with chromosomal rearrangements like translocations or inversions. These structural issues can lead to infertility, repeated miscarriages, or embryos that fail to develop. This test helps identify embryos with balanced chromosomes, increasing the likelihood of a successful pregnancy. PGT-SR offers hope for couples who have struggled with unexplained pregnancy loss or genetic complications.

Benefits of PGT

FAQS

PGT is recommended for women over 35, couples with genetic disorders, repeated miscarriages, unexplained IVF failures, or chromosomal concerns.

Embryo biopsy is performed using modern technology and highly trained embryologists, making it safe and well tolerated by embryos.

PGT reduces the risk of genetic or chromosomal issues, but no test can guarantee outcomes.

Yes. Selecting chromosomally healthy embryos often leads to higher implantation and pregnancy rates.

Genetic testing usually takes a few days, after which the results help decide the best embryo for transfer.

Take the First Step Toward a Healthy Pregnancy

Preimplantation Genetic Testing offers clarity, reassurance, and advanced support for individuals and couples seeking safe and successful fertility treatment. With precise laboratory techniques, expert genetic evaluation, and compassionate guidance, our centre is dedicated to helping you make informed decisions for your growing family.

Contact us today to schedule your PGT consultation and begin your journey toward a healthier and more confident fertility experience.

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