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Preimplantation Genetic Screening (PGS) Test

Original price was: $456.Current price is: $410.

-10%

The Preimplantation Genetic Screening (PGS) Test is a cutting-edge genetic assessment that evaluates embryos for chromosomal abnormalities before implantation during IVF treatment. Using advanced Next Generation Sequencing technology, this test analyzes embryo cells to identify numerical chromosomal abnormalities (aneuploidies) that can lead to implantation failure, miscarriage, or genetic disorders. PGS testing is particularly beneficial for women over 35, couples with recurrent pregnancy loss, those with previous IVF failures, or individuals with known genetic concerns. The test provides crucial information to help select the healthiest embryos for transfer, significantly improving pregnancy success rates and reducing the risk of chromosomal conditions. Available for $410 USD (discounted from $456 USD), this comprehensive screening offers peace of mind and informed decision-making for your fertility journey.

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Preimplantation Genetic Screening (PGS) Test

Understanding Preimplantation Genetic Screening

Preimplantation Genetic Screening (PGS) represents a revolutionary advancement in reproductive medicine that provides critical genetic information about embryos before implantation during in vitro fertilization (IVF) cycles. This sophisticated testing method allows fertility specialists to identify embryos with the correct number of chromosomes, significantly enhancing the chances of successful pregnancy and healthy baby outcomes.

PGS testing has transformed the landscape of assisted reproductive technology by offering unprecedented insights into embryo health. By screening for chromosomal abnormalities at the earliest possible stage, this test empowers couples and their medical teams to make informed decisions about which embryos to transfer, ultimately improving IVF success rates and reducing the emotional and financial burden of multiple treatment cycles.

What PGS Testing Detects and Measures

Our comprehensive PGS test utilizes state-of-the-art Next Generation Sequencing (NGS) technology to analyze embryo cells for chromosomal abnormalities, specifically focusing on:

  • Chromosomal Aneuploidies: Detection of missing or extra chromosomes that can lead to implantation failure, miscarriage, or genetic conditions like Down syndrome
  • Numerical Chromosomal Abnormalities: Comprehensive screening of all 24 chromosome pairs to ensure proper chromosomal count
  • Embryo Viability Assessment: Identification of chromosomally normal embryos with the highest potential for successful implantation and development
  • Genetic Health Evaluation: Analysis of embryo cells to determine genetic fitness before transfer

Who Should Consider PGS Testing?

Preimplantation Genetic Screening is particularly recommended for individuals and couples experiencing specific fertility challenges or risk factors:

Primary Candidates for PGS Testing

  • Advanced Maternal Age: Women aged 35 and older, where chromosomal abnormality risks increase significantly
  • Recurrent Pregnancy Loss: Couples with two or more miscarriages of unknown cause
  • Previous IVF Failures: Individuals with multiple unsuccessful IVF cycles despite good embryo quality
  • Severe Male Factor Infertility: Cases involving significant sperm abnormalities or genetic concerns
  • Family History of Genetic Disorders: Individuals with known chromosomal rearrangement carriers in the family
  • Unexplained Infertility: Couples where standard fertility evaluations have not identified the cause of infertility

Comprehensive Benefits of PGS Testing

Choosing Preimplantation Genetic Screening offers numerous advantages for your fertility journey:

Enhanced Pregnancy Success Rates

  • Improved Implantation Rates: Transfer of chromosomally normal embryos increases successful implantation by up to 60-70%
  • Reduced Miscarriage Risk: Screening eliminates embryos with chromosomal abnormalities that commonly cause pregnancy loss
  • Higher Live Birth Rates: Selection of genetically healthy embryos significantly improves chances of delivering a healthy baby

Emotional and Financial Benefits

  • Reduced Multiple Transfer Risks: Enables single embryo transfer while maintaining high success rates, minimizing multiple pregnancy complications
  • Cost-Effective Treatment: Avoids expenses associated with multiple failed IVF cycles and miscarriage management
  • Emotional Peace of Mind: Provides confidence in embryo selection and reduces anxiety about potential genetic conditions

Medical Decision Support

  • Informed Embryo Selection: Empowers fertility specialists with precise genetic data for optimal embryo transfer decisions
  • Treatment Personalization: Allows customization of IVF protocols based on individual embryo genetic profiles
  • Future Family Planning: Provides valuable information for cryopreserved embryo selection in subsequent cycles

Understanding Your PGS Test Results

Our comprehensive reporting system provides clear, actionable results to guide your fertility treatment decisions:

Result Interpretation Guidelines

  • Euploid Embryos: Embryos with the correct number of chromosomes – ideal candidates for transfer with highest implantation potential
  • Aneuploid Embryos: Embryos with chromosomal abnormalities – typically not recommended for transfer due to high risk of implantation failure or genetic conditions
  • Mosaic Embryos: Embryos containing both normal and abnormal cells – transfer decisions made in consultation with your fertility specialist based on mosaic percentage and clinical factors
  • No Result Embryos: Cases where genetic analysis was inconclusive – may require re-biopsy or alternative testing approaches

Clinical Decision Support

Your fertility specialist will interpret PGS results in the context of your complete medical history, embryo morphology, and clinical circumstances to determine the optimal transfer strategy. Results typically categorize embryos as suitable for transfer, not recommended for transfer, or requiring further discussion based on specific genetic findings.

PGS Test Pricing and Availability

Price Type Amount (USD)
Discount Price $410
Regular Price $456

Turnaround Time and Sample Requirements

  • Reporting Schedule: Samples received by Tuesday 9:00 AM – Results delivered following Tuesday
  • Sample Type: Embryo Cells collected through trophectoderm biopsy
  • Specialized Transport: Frozen embryo cells shipped in specialized transport containers available from our laboratory
  • Documentation: Completed Preimplantation Genetic Screening Consent Form (Form 23) required

Nationwide Accessibility and Support

General Genetics Corporation provides comprehensive PGS testing services across the United States, with convenient locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more cities nationwide.

Our network of experienced reproductive genetic specialists and state-of-the-art molecular diagnostics laboratories ensures consistent, reliable testing quality regardless of your location. We maintain partnerships with leading fertility clinics and reproductive centers to provide seamless integration of PGS testing into your IVF treatment plan.

Take the Next Step in Your Fertility Journey

Don’t leave your embryo selection to chance. Our Preimplantation Genetic Screening test provides the scientific certainty you need for informed reproductive decisions. With advanced NGS technology, rapid turnaround times, and comprehensive genetic analysis, we’re committed to supporting your path to parenthood.

Ready to optimize your IVF success? Contact our reproductive genetics specialists today at +1(267) 388-9828 or schedule your consultation to discuss how PGS testing can enhance your fertility treatment outcomes.

Our dedicated team is available to answer your questions, explain the testing process in detail, and coordinate with your fertility clinic to ensure smooth sample collection and timely results. Take control of your reproductive future with the confidence that comes from comprehensive genetic screening.