PRENATEST
PrenaTest is a fast, accurate, and non-invasive prenatal test that can detect the same abnormalities such as, Down Syndrome and other numerical chromosomal abnormalities as the invasive methods, without the risk to the fetus from the expecting mother’s blood.
PrenaTest is the first non-invasive German-developed test in Europe, offering individualised prenatal screening from the 9th week of pregnancy, offering three test options.
Types of PrenaTest:
PrenaTest Basic
- Screening of the Down syndrome
- Definition of the sex of the fetus
- It can also be tested in case of twin pregnancy
PrenaTest Optimum
- Screening for trisomies 21 (Down syndrome), 18 (Edwards syndrome) and 13 (Patau syndrome).
- Determining of the sex of the fetus
- Numerical abnormalities of sex (X and Y) chromosomes
- It can be performed in single and twin pregnancies
- Examination of DiGeorge syndrome (22q11.2 deletion) can be requested separately*
- This form of examination examines the most relevant abnormalities in terms of their occurrence and intrauterine identifiability, indicated by professional recommendations.
PrenaTest Plus
- It examines the entire chromosomal stock of the fetus, it provides results for numerical abnormalities of all autosomal and sex chromosomes, as well as possible duplications or deletions occurring in them, up to 7 Mb of detail
- It can be performed in single and twin pregnancies
- Examination of DiGeorge syndrome (22q11.2 deletion) can be requested separately*
PrenaTest MONOGEN
- Joint examination of PrenaTest® MONOGEN and Plus carrier screening
PrenaTest TOTAL
- Joint examination of PrenaTest® MONOGEN and ORIGIN carrier screening
It is important that before selecting any of our non-invasive genetic tests, please consult your physician or request an appointment for genetic consultation so that you can be informed as best as possible about the various tests and choose the test that best suits you. In the event of a gynecological complaint, please make an appointment with one of our obstetrician-gynecologists by clicking the button below.