PGS-PGD Testing in Lajpat Nagar Delhi
Prevent chromosomal imbalances and hereditary disorders before transfer. Our advanced Next-Generation Sequencing (NGS) screens embryos with absolute scientific precision.
Preventing Hereditary Genetic Disorders with PGT-M
When couples experience recurrent miscarriages or are carriers of serious genetic conditions, IVF cycles can carry emotional risks. Preimplantation Genetic Screening and Diagnosis (PGS/PGD) represents the most advanced genetic screening technology available. At Pravi Global IVF, we provide comprehensive, personalized care for PGS-PGD Testing in Lajpat Nagar Delhi to ensure only chromosomal-normal, healthy embryos are prioritized for transfer.
By utilizing next-generation sequencing (NGS) in our specialized genetic labs, we analyze 24 critical chromosomal pairs. This molecular level check significantly reduces miscarriage rates, boosts implantation success, and eliminates the passing down of single-gene hereditary disorders. For detailed expert video guides outlining these clinical standards, visit the Pravi IVF YouTube Channel.
Preimplantation Genetic Testing for Chromosomal Aneuploidy (PGT-A)
Understanding our specialized genetic screening options enables couples to make highly informed clinical decisions:
PGT-A (Aneuploidy Screening)
Checks for abnormal chromosome counts (like Down Syndrome or Trisomies). This is highly recommended for advanced maternal age or recurrent miscarriage cases.
PGT-M (Monogenic/Single Gene Screening)
Targets specific inherited single-gene conditions such as Thalassemia, Cystic Fibrosis, or Hemophilia, preventing hereditary transfer.
PGT-SR (Structural Rearrangements)
Assesses chromosomal translocations or inversions, ensuring normal structural chromosome karyotypes in selected embryos.
Tailored Embryo Biopsy and NGS Lab Stage Protocols
To perform genetic screening safely, we culture embryos to the advanced Day 5 blastocyst stage. Culturing to this stage allows our senior embryologists to harvest 3 to 5 cells from the trophectoderm (which later forms the placenta) using an ultra-precise micro-laser, ensuring the inner egg mass remains untouched.
The biopsied embryos are safely vitrified (flash-frozen) while our geneticist screens the genetic files. The chromosomal-normal embryos are subsequently mapped for transfer during a precise IVF treatment cycle.
Book Consult
Schedule a baseline diagnostic consult with our genetic and clinical embryology panel to discuss your screening options.
Book via GoogleCall Genetics LabLab Standards
- Next-Generation Sequencing (NGS) platforms.
- Micro-laser biopsying under absolute stability.
- Complete genetic counseling support.
- Day 5 blastocyst culture standard.
PGS-PGD Testing in Lajpat Nagar Delhi FAQ
What is the primary difference between PGS and PGD?
PGS (now PGT-A) screens for chromosomal count errors such as Down Syndrome. PGD (now PGT-M) diagnoses specific inherited genetic disorders such as Thalassemia or Cystic Fibrosis when parents are known carriers.
What is the cost of PGS-PGD testing in lajpat nagar delhi?
Genetic screening involves highly advanced molecular NGS platforms and embryology biopsying, priced per embryo. Please contact our front desk directly for detailed pricing sheets.
Can embryo biopsying harm the developing embryo?
Biopsying is performed strictly at the blastocyst stage (Day 5), harvesting only trophectoderm cells (placenta cells). The inner cell mass remains untouched, ensuring zero harm to developmental potential.
Are the success rates of IVF higher with PGS-PGD screening?
Yes, significantly. By ensuring only genetically normal and healthy embryos are prioritized for transfer, it cuts miscarriage rates and raises success rates per transfer.
Absolute Genetic Verification for a Healthy Family Future
Empower your reproductive plans with absolute clinical safety and next-generation sequencing validation.