Get best Advancing IVF and Genetic Insight with Preimplantation Genetic Testing PGT
                     Advancing IVF and Genetic 
Insight with 
Preimplantation Genetic 
Testing
About Us
Grace Fertility and Reproductive Medicine is committed to 
ensuring families are created by being supported, informed, and 
treated with compassion. We take the time to learn about our 
patients—who they are; what type of health issues they have; 
what their goals are; what their unique journey through 
infertility is—and recommend a treatment method that meets 
each patient's needs. Our staff has extensive knowledge of all 
aspects of reproductive medicine, from straightforward cases of 
infertility to the most complicated reproductive problems, and is 
dedicated to helping patients find clarity and understand every 
step of the process.
Innovative IVF Enhancements & Prenatal 
Screening
For a greater chance of achieving a successful pregnancy, we provide advanced fertility enhancement and prenatal 
screening options such as Preimplantation Genetic Testing (PGT). Our specialists evaluate your individual situation 
throughout your fertility journey to determine the most appropriate and beneficial reproductive techniques, like 
Preimplantation Genetic Testing (PGT), based on your unique circumstances and preferences.
Every patient's path is unique. Our comprehensive approach combines state-of-the-art genetic testing with 
compassionate, personalized care to maximize your opportunities for a healthy pregnancy and baby.
Preimplantation Genetic Testing – PGT-A
What is PGT-
A?
Preimplantation Genetic Testing for Aneuploidy (formerly known as 
PGS) is an advanced screening method that identifies embryos with 
chromosomal abnormalities before transfer.
This precise testing examines all 23 chromosome pairs, ensuring only 
embryos with the correct number of chromosomes are selected for 
implantation.
Preimplantation Genetic Testing – PGT-M
Screening for Inherited Conditions
PGT-M (Preimplantation Genetic Testing for Monogenic Disorders) screens 
embryos for specific inherited genetic conditions with at least 90% accuracy, 
providing peace of mind for families with known genetic risks.
This powerful test can identify single-gene disorders before pregnancy, 
allowing you to make informed decisions about embryo selection.
Who Should Consider PGT-M?
Cystic Fibrosis Fragile X Syndrome
Affects respiratory and digestive systems Leading inherited cause of intellectual disability
EMBRACE – Non-Invasive Embryo 
Screening
Revolutionary Gentle No Embryo Biopsy 
Testing Required
EMBRACE (Embryo Analysis of Culture Completely non-invasive 
Environment) represents a approach preserves embryo 
breakthrough in genetic screening. This integrity
innovative method analyzes DNA 
Identifies Chromosomally 
released naturally into the embryo's Normal Embryos
culture medium—without any physical 
contact with the embryo itself.
Accurate screening for optimal 
selection
Maximizes Pregnancy 
Success
Helps achieve the best possible 
outcomes
Endometrial Receptivity Analysis (ERA)
Optimizing Implantation Timing
ERA is an advanced diagnostic tool that identifies the timing of peak 
receptivity of the endometrium for embryo implantation (implantation 
window). It is often used in conjunction with 
preimplantation genetic testing (PGT) to increase the success rates of 
IVF.
Who Benefits from ERA?
This test is particularly valuable for patients who have experienced 
repeated implantation failures despite transferring high-quality 
embryos.
Personalized Improved Success Rates
Timing
Identifies your unique receptive implantation window with precision Significantly increases chances of successful embryo attachment and 
pregnancy
Non-Invasive Prenatal Testing (NIPT – Harmony)
NIPT is a safe, simple blood test that can be performed as early as 10 weeks into pregnancy, 
providing valuable insights into your baby's chromosomal health without any risk to your 
pregnancy.
Exceptional 
Accuracy
What NIPT Screens 
For 99%
Trisomy 
D21own syndrome
Trisomy Detection 
1 RateEd8wards syndrome For trisomy 21 (Down syndrome)
Trisomy 
P1a3tau syndrome
0.15%
False Positive 
Rate
Remarkably low across all conditions
Why Choose 
NIPT?
Understanding Trisomies
Chromosome 
Humans typically have 23 pairs of 21
Down Syndrome
chromosomes—46 total. A trisomy occurs 1
when an extra copy of a chromosome is Most common trisomy, affecting 
present, resulting in three copies instead intellectual development and 
physical features
of two.
These additional chromosomes can lead to 
Chromosome 
various developmental and health 18
challenges. NIPT provides early, reliable 2 Edwards Syndrome
insights into fetal chromosomal health, Affects multiple organ systems 
giving you the information you need to with serious health implications
prepare and make informed decisions.
Chromosome 
13
3 Patau Syndrome
Severe developmental 
abnormalities affecting brain and 
heart
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