Prenatal Testing
Preconception Genetic Evaluation
& Carrier Testing
Comprehensive genetic testing for worry-free
pregnancy and peace of mind
By combining Bionano Optical Genome Mapping technology with Whole Genome and Transcriptome Sequencing, Praxis Genomics is unique in offering genome-wide carrier testing with functional evaluation of the findings to identify the cause of infertility or genetic disorders that could affect the child.
This is the most sensitive and specific genetic testing available anywhere in the world and covers all types of genetic variants that go undetected by standard carrier testing. This combination testing allows a worry-free pregnancy and peace of mind for the future health of the child.
Non-Invasive Prenatal Testing (NIPT)
Non-Invasive Prenatal Testing (NIPT) is commonly used to screen for chromosomal abnormalities early in pregnancy. However, pregnant women often face the issue of inconclusive NIPT results. These can be especially worrisome when there is a history of complicated and failed pregnancies or previous children with developmental problems.
Learn More About NIPT Testing
Non-Invasive Prenatal Testing (NIPT)
Single Carrier Testing
Single Carrier Testing provided by Praxis ensures that both parents can produce healthy gametes (sperm or eggs). These tests identify the potential causes of infertility as well as inherited conditions that might be transmitted to future children.
Learn More About Carrier Individual Testing
Single Carrier Testing
Couple Carrier Testing
Couple Carrier Testing identifies recessive conditions which may affect the child, or result in repeated pregnancy losses.
For couples with fertility problems, in vitro fertilization (IVF) is an incredible option but it doesn't guarantee a successful pregnancy. One of the key hurdles is ensuring the genetic health of parents, as many IVF cycles result in early miscarriages or failed pregnancies due to undetected parental genetic abnormalities.
Genome Testing, offered in partnership with Praxis, can significantly improve IVF outcomes by identifying potential risks early and ensuring that only the healthiest embryos are transferred.
Learn More About Carrier Couple Testing
Couple Carrier Testing
Inconclusive Ultrasound Results
Inconclusive Ultrasound Results
Families may experience inconclusive ultrasound results which may or may not indicate fetal abnormalities or severe health defects. Praxis can exclude the most common causes of such findings and provide reassurance to families regarding the future of the pregnancy.
Learn More About Prenatal TestingConditions Screened For
We screen for common genetic conditions caused by extra or missing chromosomes in the baby's DNA. Using unique technology to distinguish between the pregnant person's and the baby's DNA, we can test for a comprehensive range of conditions including triploidy.
Trisomies
Trisomy 21 (Down syndrome)
Trisomy 18 (Edwards syndrome)
Trisomy 13 (Patau syndrome)
Sex Chromosome Aneuploidies
Monosomy X (Turner syndrome)
XXY Syndrome (Klinefelter Syndrome)
Triple X syndrome
XYY Syndrome (Jacob's Syndrome)
Microdeletions
22q11.2 deletion syndrome
Prader-Willi syndrome
Angelman syndrome
1p36 deletion syndrome
Cri-du-chat syndrome
Triploidy
Only NIPT that tests for triploidy
Triploidy
Ready to Get Started?
Reach out today to book a free consultation with our Medical Director and team of experts
Phone: (678) 837-4022
Hours: Monday - Friday, 8AM - 6PM