Guide your patients with genetic insights during a special time in their life: their pregnancy.
The Prequel® Prenatal Screen is designed to provide individualized insights for each patient, so you can seamlessly and consistently incorporate prenatal genetic screening into your practice. This means more of your patients will benefit from valuable information that can make a difference in health outcomes for families.
Prequel with AMPLIFY delivers results to 99.9% of patients on the first draw regardless of ancestry or body mass index (BMI).1 Why is that important?
Watch this patient story to hear how noninvasive prenatal screening can give a patient like Hannah, early insights into her pregnancy to help prepare her family.
Screening at 10 weeks gives you and your patient time to explore different options such as:
Meet with your patient to discuss non-invasive prenatal screening.
Submit the completed Test Request Form (TRF) and sample.
Receive Prequel results in approximately 7-10 days.
Review results with patient.
Refer patients to schedule a consultation with Myriad’s Certified Genetic Counselors.
The Prequel® Prenatal Screen with AMPLIFY™ technology is a non-invasive prenatal screen that uses cell-free DNA (cfDNA) to determine if a pregnancy is at an increased risk for common chromosome abnormalities, such as Down Syndrome (Trisomy 21), Turner Syndrome (Trisomy 18), and Patau Syndrome (Trisomy 13).
cfDNA screening has been shown to be superior to methods that use maternal age, ultrasound, and serum screening6, and results in a lower false-positive rate and false-negative rate. That translates to a lower chance of needing a repeat test or an invasive diagnostic procedure. We use advanced science and technology that works for any pregnancy regardless of age, including those with twin and IVF pregnancies.
The Prequel Prenatal Screen can be ordered together with the Foresight® Carrier Screen and offered to any pregnant person. Prequel can provide individual fetal sex information for twins, in addition to singleton pregnancy.
Included with every screen: Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome), Trisomy 13 (Patau syndrome)
We provide resources to help educate your patients about Myriad products.
We offer a comprehensive program to make genetic products accessible for more of your patients.
We deliver screening and testing results effectively and thoroughly so you can focus on care plans.
We provide consults from patient educators, who are genetic counselors, tailored to help address any questions your patients may have.