PANORAMA® TEST

NIPT – NON INVASIVE PRENATAL TEST

Why get tested?

The non-invasive prenatal genetic screening test allows to evaluate the risk of the main aneuploidies and some fetal chromosomal microdeletions, with a simple blood sample.
The test is indicated for all pregnant women and, in particular, for women over the age of 35 who have an increased risk of having a fetus affected by the main aneuploidies and some fetal chromosomal microdeletions.

What the test detects

We offer different types of tests available:
Panorama® Basic: Test for Trisomy 21, Trisomy 18, Trisomy 13, Aneuploidy of sex chromosomes, Triploidy + Analysis of fetal sex.
Panorama® Medium: Test for Trisomy 21, Trisomy 18, Trisomy 13, Sex chromosome aneuploidy, Triploidy, Deletion syndrome 22q11.2 + Fetal sex analysis.
Panorama® Full: Test for Trisomy 21, Trisomy 18, Trisomy 13, Sex chromosome aneuploidy, Triploidy, 22q11.2 Deletion Syndrome, 1p36 Deletion Syndrome, ‘Cri du Chat’ Syndrome, Angelman Syndrome, Prader Syndrome- Willi + Fetal Sex Analysis.
Twin Panorama® Basic: test for Trisomy 21, Trisomy 18, Trisomy 13.
Twin Panorama® Medium: test for Trisomy 21, Trisomy 18, Trisomy 13, aneuploidy of the sex chromosomes, -deletion syndrome 22q11.2.
Panorama® Basic egg donation: test for Trisomy 21, Trisomy 18, Trisomy 13.

What variants cause

Variants produce a high probability of high risk.

How testing works

The genetic test consists of performing a blood sample, extracting free circulating DNA and analyzing free fetal DNA circulating in maternal blood using Next Generation Sequencing (NGS) techniques and sophisticated bioinformatics analyzes.

Reporting time

For Panorama® Basic, Medium and Full from 5 to 7 working days. For Twin Panorama® Basic, Twin Panorama® Medium and Panorama® Basic Egg Donation: about 10 working days.

Sensitivity and specificity

Analytical sensitivity 93.8 – 99% and analytical specificity > 99%.

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