PANORAMA® Test
Panorama prenatal screening is a safe, accurate and painless blood-based prenatal DNA screening test (NIPT) that checks your baby for chromosome conditions by analysing abnormalities in the DNA. The Panorama test screens for a wide range of abnormalities.
Reliable and unique genetic screening that:
- is able to screen the most common fetal chromosomal abnormalities from the expecting mother’s blood
- distinguishes between maternal and fetal DNA
- Suitable for screening for Down Syndrome and other chromosome abnormalities
- can be performed from the 9th week of pregnancy and in case of twin pregnancies.
Optional screening tests:
Panorama® PLUS test
The package consist of:
Down syndrome |
Edwards syndrome |
Patau syndrome |
Triploidy, Disappearing twin syndrome |
Sex of the fetus (optional) |
Klinefelter syndrome (XXY) |
Triple X syndrome (XXX) |
Turner syndrome |
Jacob syndrome |
Genetic consultancy |
Diagnostic confirmation in case of high risk |
It can be done from the 9th week of pregnancy |
Distination between fetal and maternal genetic stock |
Also in case of twin pregnancy and egg donation |
Price:
189.000 HUF |
Panorama® +22q test
The package consist of:
Down syndrome |
Edwards syndrome |
Patau syndrome |
Triploidy, Disappearing twin syndrome |
Sex of fetus |
Klinefelter syndrome (XXY) |
Triple X syndrome (XXX) |
Turner syndrome |
Jacob syndrome (XYY) |
DiGeorge syndrome |
Genetic counseling |
Diagnostic confirmation in case of high risk |
Also in case of twin pregnancy |
It can be done from the 9th week of pregnancy |
Real distination between fetal and maternal genetic stock |
Ár:
209.000 HUF |
Panorama® EXTRA test
The package consist of:
Down syndrome |
Edwards syndrome |
Patau syndrome |
Triploidy, Disappearing twin syndrome |
Sex of fetus |
Klinefelter syndrome (XXY) |
Triple X syndrome (XXX) |
Turner syndrome |
Jacob syndrome (XYY) |
DiGeorge syndrome |
Cri-du-chat syndrome |
Angelman syndrome |
Prader-Willi syndrome |
1p36 deletion syndrome |
Genetic consultancy |
Diagnostic confirmation in case of high risk |
It can be done from the 9th week of pregnancy |
Distination between fetal and maternal genetic stock |
Ár:
239.000 HUF |
