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Preimplantation Genetic Screening (PGS) Per Embryo

Original price was: $400.Current price is: $300.

-25%

Preimplantation Genetic Screening (PGS) per embryo is a cutting-edge genetic test that analyzes embryos created through in vitro fertilization (IVF) for chromosomal abnormalities before implantation. This comprehensive screening evaluates all 24 chromosomes to identify embryos with the correct number of chromosomes, significantly increasing the chances of successful pregnancy and reducing miscarriage risks. Using advanced Next-Generation Sequencing (NGS) technology, PGS provides detailed chromosomal analysis to help select the healthiest embryos for transfer. The test is particularly beneficial for couples experiencing recurrent pregnancy loss, advanced maternal age, or previous IVF failures. At just $300 USD, this test offers invaluable insights for optimizing IVF outcomes and building healthy families.

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Preimplantation Genetic Screening (PGS) Per Embryo

Comprehensive Genetic Screening for IVF Success

Preimplantation Genetic Screening (PGS) per embryo represents a revolutionary advancement in reproductive medicine, offering couples undergoing in vitro fertilization (IVF) the opportunity to screen embryos for chromosomal abnormalities before implantation. This sophisticated genetic testing method provides critical information that can significantly improve pregnancy success rates and reduce the risk of miscarriage.

What Does PGS Testing Measure?

PGS testing utilizes state-of-the-art Next-Generation Sequencing (NGS) and microarray technology to comprehensively analyze all 24 chromosomes in each embryo. The test specifically detects:

  • Chromosomal aneuploidies (abnormal number of chromosomes)
  • Trisomies (extra chromosomes)
  • Monosomies (missing chromosomes)
  • Structural chromosomal abnormalities
  • Mosaic embryos (mixed normal and abnormal cells)

By identifying embryos with the correct chromosomal complement, PGS helps select the most viable embryos for transfer, increasing the likelihood of successful implantation and healthy pregnancy.

Who Should Consider PGS Testing?

Preimplantation Genetic Screening is particularly recommended for:

  • Advanced Maternal Age: Women aged 35 and older, where chromosomal abnormality risks increase significantly
  • Recurrent Pregnancy Loss: Couples experiencing multiple miscarriages
  • Previous IVF Failures: Individuals with unsuccessful IVF cycles despite good embryo quality
  • Severe Male Factor Infertility: Cases with poor sperm parameters
  • Family Building with Known Genetic Concerns: Couples wanting to maximize their chances of a healthy pregnancy
  • Single Embryo Transfer Candidates: Patients opting for elective single embryo transfer

Key Benefits of PGS Testing

Enhanced IVF Success Rates

PGS testing significantly improves pregnancy rates per transfer by identifying chromosomally normal embryos, which have higher implantation potential compared to abnormal embryos.

Reduced Miscarriage Risk

By transferring only chromosomally normal embryos, PGS dramatically decreases the risk of miscarriage, as most early pregnancy losses are caused by chromosomal abnormalities.

Shorter Time to Pregnancy

PGS helps avoid transferring embryos that would not result in pregnancy, potentially reducing the number of IVF cycles needed to achieve a successful pregnancy.

Informed Family Planning Decisions

The comprehensive chromosomal information provided by PGS empowers couples and their fertility specialists to make informed decisions about embryo selection and treatment planning.

Understanding Your PGS Results

Normal (Euploid) Results

Embryos classified as euploid contain the correct number of 46 chromosomes and are considered optimal for transfer. These embryos have the highest potential for successful implantation and healthy development.

Abnormal (Aneuploid) Results

Aneuploid embryos contain an incorrect number of chromosomes and are typically not recommended for transfer due to high risks of implantation failure, miscarriage, or genetic disorders.

Mosaic Embryos

Some embryos may show mosaic patterns, containing both normal and abnormal cells. The transfer decision for mosaic embryos requires careful consideration and discussion with your fertility specialist.

Inconclusive Results

In rare cases, results may be inconclusive due to technical factors. Your fertility team will guide you on the appropriate next steps.

PGS Testing Process and Timeline

The PGS testing process involves embryo biopsy at the blastocyst stage (typically day 5-7 of development), where a few trophectoderm cells are carefully removed for analysis. The biopsied cells are then analyzed using advanced NGS technology, with results typically available within 1-2 days, allowing for timely embryo transfer decisions.

Test Pricing Information

Test Name Discount Price Regular Price
Preimplantation Genetic Screening (PGS) Per Embryo $300 USD $400 USD

Nationwide Availability

We have branches across the United States, serving patients in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our comprehensive network ensures accessible, high-quality genetic testing services nationwide.

Take the Next Step Toward Your Family Goals

Don’t leave your IVF success to chance. Preimplantation Genetic Screening provides the scientific insight needed to make informed decisions about your embryo transfer. Our experienced genetic counselors and fertility specialists are ready to guide you through the process and help you achieve your dream of building a healthy family.

Book Your PGS Test Today!
Call or WhatsApp: +1(267) 388-9828
Our dedicated team is available to answer your questions, discuss your specific situation, and schedule your PGS testing.

Note: Preimplantation Genetic Screening/PGS (per embryo) requires a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.