About the test

TRISOMY test is a non-invasive, safe and painless screening test from the future mother’s blood, which can exclude with great precision the presence of fetal chromosomal disorders starting from the 11th week of pregnancy. If you wish, the test may also identify the fetal sex. Before ordering the test, it is required that you read the latest version of the Information Concerning Genetic Laboratory Testing.

The price of the test

350 €

What does the test reveal?

The test excludes frequent disorders in the number of fetal chromosomes 21, 18 and 13 (the cause of Down, Edwards and Patau syndromes).

Reveals possible false positive results of biochemical prenatal screening.

Minimizes the need for amniocentesis (invasive amniotic fluid collection).

Determines the fetal sex, if you are interested.

TRISOMY test may be taken by a pregnant woman at her own request and after a genetic consultation. The test is suitable for any pregnant woman starting from the 11th week of pregnancy if:

TRISOMY test can also be applied in twin pregnancies, however, in the event of a pathological finding, it is not possible to attribute the finding from the test result directly to a particular fetus of the twins.

Test overview