At clinique ovo near Côte-des-Neiges, we offer the Harmony test, a non-invasive prenatal screening that detects chromosomal conditions and determines your baby’s sex from 10 weeks of pregnancy. This advanced test provides accurate and reliable results, giving you peace of mind in a calm and private environment.
At clinique ovo near Côte-des-Neiges, we offer the Harmony test, a non-invasive prenatal screening that analyzes fetal DNA in maternal blood to detect trisomy 13, 18, and 21, as well as sex chromosome abnormalities and fetal sex. This simple blood test, performed from 10 weeks of pregnancy, significantly reduces the need for invasive procedures like amniocentesis and chorionic villus biopsy. Results are available within 5 to 11 working days, providing expecting parents with reliable and accurate information early in pregnancy.
Excitingly, the Harmony test is now performed in Quebec, making clinique ovo’s medical analysis laboratory the first and only Quebec facility to offer this screening. A team of accredited experts analyzes the test in state-of-the-art laboratories, ensuring the highest standards of precision and reliability.
With a detection rate of over 99.9% for trisomy 21 and approval by Health Canada, Harmony offers expectant parents peace of mind with safe and accurate prenatal screening.
Supporting your prenatal well-being
Let the ovo prenatal team help you ensure a healthy pregnancy.
When you come to clinique ovo, you will benefit from the expertise and complete attention of our medical team. We will support you through your process and do everything possible to make your experience positively memorable.
Tuesday, September 26 at 7:00 p.m. by Laurence Filion-Cloutier, clinical advisorDo you have questions about umbilical cord blood stem cells? Do you want to know the benefits of these precious cells? Follow our free information session to learn more learn more!
Reduce the risk of transmitting a genetic condition to your child.
We are all carriers of several genetic changes without knowing it, and 4% of couples have a significant risk of transmitting a genetic condition to their child, even in the absence of a family history.Do you want to know the risk in your situation? A simple blood test could tell you more.
