myPrenatal basic

myPrenatal basic – this is a non-invasive prenatal test (NIPT) intended for the detection of trisomies of chromosomes 21, 18, and 13. If the pregnant woman wishes, the fetal sex is indicated. In the case of a twin pregnancy, it is possible to determine whether at least one of the fetuses has a Y chromosome, i.e., is male.
The NIPT test is based on the analysis of free fetal DNA, using whole genome sequencing (WGS). In the cell-free DNA (cfDNA) circulating in the pregnant woman's blood, a fraction of the placenta(s) DNA (cffDNA) of the fetus(es) is detected.

Recommendation from when to conduct the test: Singleton and twin - from 10 weeks of pregnancy.

Sample: blood.

Time to completion after arrival in the laboratory: 2-4 working days.