TRISOMY test +

About the test

TRISOMY test + is a genetic laboratory test with additional features that can detect more chromosomal disorders compared to TRISOMY test and TRISOMY test XY. It identifies the risk of trisomy of chromosomes 21, 18 and 13, disorders in the number of sex chromosomes and selected chromosomal microdeletions which represent conditions where a part of a chromosome is missing. TRISOMY test + also determines the chromosomal sex of the fetus. 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

450 €

What will the test reveal?

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

It excludes possible aberrations in the number of sex chromosomes (the cause of Turner syndrome 45,X; Klinefelter syndrome XXY and XYY and XXX Syndromes).

It excludes the possibility of selected chromosomal deletions (the cause of DiGeorge syndrome 22q11, 1p36 deletion syndrome,
Prader-Willi and Angelman syndrome, Cri-du-chat syndrome, Wolf-Hirschhorn syndrome).

It will also reveal any possible false positive results of biochemical prenatal screening.

It minimizes the need for amniocentesis (invasive amniotic fluid collection).

If you are interested, the test can determine the sex of the fetus.

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

TRISOMY test + cannot be used in multifetal pregnancies.

Test overview