General Information About the Test
The Fetal DNA Test, also known as NIPT (Non-Invasive Prenatal Test), is a revolutionary genetic screening test in which free-floating DNA fragments belonging to the baby circulating in the mother's blood are isolated and examined using a simple blood sample taken from the expectant mother's arm. It allows for the detection of many chromosomal anomalies, primarily Down Syndrome (Trisomy 21), with an accuracy of over 99%, without the need for invasive procedures that carry a risk of miscarriage, such as amniocentesis.
Test Process and Preparation
Administration of the Fetal DNA test and gestational week planning.
In which week of pregnancy can the test be performed?
It can be safely performed at any time from the 10th week of pregnancy onwards, when the amount of fetal DNA in the mother's blood reaches a sufficient level.
Does it pose any harm to the baby or the mother?
It has absolutely no harm and carries no risk of miscarriage (cardiac or bleeding). It is performed merely via a standard blood draw from the mother (just like a routine blood test).
How long does it take to get the test result?
Because the collected blood sample is sequenced with highly sensitive instruments in high-tech genetic laboratories (mostly in centers abroad), it can take an average of 7 to 14 days for the results to be ready.
The information on this page is for informational purposes only. The results of medical tests must be evaluated by specialist physicians.
