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.
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
Panorama® +22q 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
- Real distination between fetal and maternal genetic stock
- DiGeorge syndrome
- Az USA-ban ez a csomag válik már az alapcsomaggá.
Panorama® EXTRA 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
- DiGeorge syndrome
- Cri-du-chat syndrome
- Angelman syndrome
- Prader-Willi syndrome
- 1p36 deletion syndrome