PANORAMA® TEST PACKAGES
The Panorama prenatal screening s 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
Screening for Down, Edwards, Patau syndromes and sex chromosome abnormalities
- Down syndrome
- Edwards syndrome
- Patau syndrome
- Triploidy, Disappearing twin syndrome
- Sex of the fetus (optional)
- Klinefelter syndrome (XXY)
- Triple X syndrome (XXX)
- Turner syndrome (X monosyndrome)
- Jacob syndrome (XYY)
- GENETIC ULTRASOUND
- Diagnostic confirmation in case of high risk
- It can be done from the 9th week of pregnancy
- Distination between fetal and maternal genetic stock
PANORAMA® +22Q TEST
Screening for DiGeorge, Down's, Edwards, Patau syndromes and sex chromosome abnormalities
- Down syndrome
- Edwards syndrome
- Patau syndrome
- Triploidy, Disappearing twin syndrome
- Sex of the fetus (optional)
- Klinefelter syndrome (XXY)
- Triple X syndrome (XXX)
- Turner syndrome (X monosyndrome)
- Jacob syndrome (XYY)
- GENETIC ULTRASOUND
- 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
- In the US, this package is now becoming the basic package.
PANORAMA® EXTRA TEST
Screening for microdeletion syndromes, Down's, Edwards, Patau syndromes and sex chromosome abnormalities
- Down syndrome
- Edwards syndrome
- Patau syndrome
- Triploidy, Disappearing twin syndrome
- Sex of the fetus (optional)
- Klinefelter syndrome (XXY)
- Triple X syndrome (XXX)
- Turner syndrome (X monosyndrome)
- Jacob syndrome (XYY)
- GENETIC ULTRASOUND
- 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
It is important that before you choose any of our non-invasive genetic tests, please consult your doctor or make an appointment for a genetic counselling session to find out more about the different tests and to choose the test that is best for you.