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What exactly is NIPT?
Non-invasive prenatal screening (NIPT) uses cell-free DNA (cfDNA) produced by the maternity to gauge feasible chromosomal conditions in a maternity. NIPT is just a prenatal assessment test which can be done as soon as 10 months of being pregnant utilizing a blood draw that is single. Prenatal tests that are diagnostic as amniocentesis and CVS diagnose the existence of chromosomal conditions. They’ve been typically done later on in maternity as they are related to a little chance of maternity loss.
Why display screen for chromosomal conditions?
Chromosomal conditions such as for example Down problem can impact handling of your maternity and distribution as well as the wellness of the newborn.
These conditions sometimes happens in just about any pregnancy- even if there’s no grouped family members history- simply because they typically aren’t inherited. They happen by “chance”, and even though the chance increases with mom’s age, many children with chromosomal conditions are born to females under 35 years old. 1
That’s why the United states College of Obstetricians and Gynecologists (ACOG) suggests that most expecting women be provided assessment and diagnostic tests for chromosomal conditions. 2 And since NIPT is one of screening that is sensitive for trisomies 21, 18, and 13, the Global Society for Prenatal Diagnosis (ISPD) supports providing NIPT to all or any expecting mothers. 3
Your prenatal screening results can offer both you and information specific to your pregnancy to your doctor in order to do have more informed conversations regarding the prenatal care. Continue Reading →