HARMONY PRENATAL TEST Innovative non-invasive prenatal test that detects major trisomies with 99% certainty The mother and the fetus must be attended to throughout the pregnancy, which is why the prenatal screening, a series of analyzes and ultrasound data that determine the risk of the fetus being affected by a specific anomaly, is an essential and decisive step in a pregnancy , allowing expectant mothers to feel they are in a safe pregnancy

The Combined 1st Trimester Screening, an early test that combines the information from the ultrasound and biochemical examinations, and evaluates the degree of risk for the existence of the Trisomy 21 (Down Syndrome), Trisomy 18 (Edwards Syndrome) and Trisomy 13 of Patau), appears as the most common screening method, with a detection rate of about 90 to 97% However, the notorious scientific and technological advance in the prenatal diagnosis introduced the Harmony PreNatal Test, which constitutes the latest progress in this area It is a noninvasive test for the screening of the three major Trisomies (T21, 18, 13) and aneuploidies related to the sex chromosomes (X and Y) and is performed simply and safely, using a sample of maternal peripheral blood and allows obtain results with a high degree of accuracy It is the non-invasive prenatal screening test that has the highest detection rates (> 99%) for the major trisomies It is available for all pregnant women from 10 weeks of pregnancy, being a 100% safe method, with total absence of risk for the baby and with aneuploidy detection rates very close to those of diagnostic methods (amniocentesis and biopsy of chorionic villi )


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