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 |
