The Non Invasive Prenatal Test for detecting fetal chromosomal abnormalities during pregnancy

Prenatalsafe® provides detailed information on the baby’s health before birth.

The Non Invasive Prenatal Test for detecting fetal chromosomal abnormalities during pregnancy

Prenatalsafe® provides detailed information on the baby’s health before birth.

Prenatal Screening Tests

Prenatal Screening Tests are analyses performed during pregnancy to assess the health of the fetus.

These tests allow early detection of diseases associated with DNA variants and abnormalities in the number or structure of chromosomes.

Being informed is the first step to obtaining assistance in childbirth or to initiating, when possible, a course of treatment before or immediately after the birth of the child.

Prenatalsafe Eurofins Genoma

Prenatalsafe®, the innovative non-invasive prenatal test to detect chromosomal abnormalities and genetic diseases directly on the fetus, is the result of Eurofins Genoma’s OrizzonteNascita project.

Prenatalsafe® is the most complete non-invasive prenatal screening test that analyzes fetal DNA extracted from a maternal blood sample.

It allows you to identify the presence of abnormalities in chromosomes, both in number (aneuploidies) and in structure. Abnormalities that are the basis of some of the most common genetic diseases.

It offers 9 levels of depth, thanks to which it is possible to obtain an extremely complete informational picture starting from the 10th week of pregnancy.

What are aneuploidies?

Aneuploidies are genetic abnormalities, characterized by a higher or lower number of chromosomes than the standard number, leading to deficits or disabilities.

How is it done?

the Prenatalsafe® test is performed with a simple maternal blood sample.

Prenatalsafe® minimizes the risks of abortiveness related to traditional invasive prenatal diagnostic techniques, such as amniocentesis and chorionic villus sampling.

Simple

A simple mother’s blood sample is required at the 10th week of gestation.

Safe

It is a non-invasive test, reducing the risks of abortion present in traditional invasive prenatal diagnostic techniques, such as amniocentesis and villocentesis.

Fast

Thanks to the high-resolution FAST protocol, test results will be available after just 3 working days.

Complete

It is 99.9% reliable. It can detect anomalies even if there is a low amount of fetal DNA in maternal blood, unlike other tests that require a higher amount of fetal DNA.

Clear Results

Definite outcome: positive or negative test result

Prenatalsafe® is available in 9 versions, each with a different level of depth.

It is available throughout Italy and the analyses are performed at the Eurofins Genoma laboratories in Milan, Rome and Florence.

3

Evaluates the aneuploidies of chromosomes 21 (Down syndrome), 18 (Edwards syndrome), 13 (Patau syndrome), and includes the determination of fetal sex (optional).

5

Evaluates the aneuploidies of chromosomes 21 (Down syndrome), 18 (Edwards syndrome), 13 (Patau syndrome) and sex chromosomes, and includes the determination of fetal sex (optional).

5DiGeorge

Evaluates the aneuploidies of chromosomes 21 (Down syndrome), 18 (Edwards syndrome), 13 (Patau syndrome), sex chromosome aneuploidies and the microdeletion of chromosome 22 (DiGeorge syndrome).

Plus

In addition to what is provided by the Prenatalsafe® 5 test, it also includes the option for further investigation to identify trisomy of chromosomes 9 and 16 and the presence of structural chromosomal alterations, i.e. 6 of the most common microdeletion syndromes.

Karyo

Detects fetal aneuploidies and structural chromosomal alterations in every chromosome (deletions and segmental duplications).

Karyo Plus

Adds the study of 9 of the most common microdeletion syndromes to the capabilities of Prenatalsafe® Karyo.

Complete

It is one of the most technologically advanced non-invasive prenatal tests.

By analyzing the circulating fetal DNA in maternal blood, it is capable of performing the fetal karyotype screening and serious fetal genetic diseases.

Complete Plus

Adds the study of 9 of the most common microdeletion syndromes to the capabilities of Prenatasafe® Complete.

Full risk

Adds the Genescreen® focus test, a carrier screening for both parents that identifies mutations related to recessive hereditary diseases that can potentially be transmitted to the fetus, to the benefits of Prenatasafe® Complete Plus.

A complete and innovative non-invasive prenatal test, suitable for any different need.

Who we recommend Prenatalsafe® to

The Prenatalsafe® examination is the best test in the following cases:

Pregnancies in which prenatal invasive diagnosis is contraindicated (e.g. risk of spontaneous abortion)

First trimester (bi-test) positive

Advanced maternal age (>35 years)

Advanced paternal age (>40 years)

Previous cases of chromosomal anomalies in the family

Parent carrying a balanced translocation

Prenatalsafe® tests can be performed starting from the 10th week of gestation (calculated from LMP) and every future mother can undergo the tests.

Eurofins Genoma offers free consulting to advise on the most appropriate analysis for each couple’s needs.

Prenatalsafe® is useful in the following cases:

Single
pregnancies

Obtained through natural conception or assisted fertility techniques.

Twin
pregnancies

Obtained through natural conception or assisted fertility techniques.

Previous
miscarriages

Pregnancies ended with spontaneous abortion or voluntary interruption.

Get your results in record time:

TestTurnaround Time
Prenatalsafe® 33 business days
Prenatalsafe® 53 business days
Prenatalsafe® 5DiGeorge3 business days
Prenatalsafe® Plus5 to 7 business days
Prenatalsafe® Karyo4 to 5 business days
Prenatalsafe® Karyo Plus5 to 7 business days
Prenatalsafe® COMPLETE4 to 15 business days
Prenatalsafe® COMPLETE Plus5 to 15 business days
Prenatalsafe® FULL RISK5 to 20 business days

Test

Prenatalsafe® 3

Turnaround Time: 3 business days

Prenatalsafe® 5

Turnaround Time: 3 business days

Prenatalsafe® 5DiGeorge

Turnaround Time: 3 business days

Prenatalsafe® Plus

Turnaround Time: 5 to 3 business days

Prenatalsafe® Karyo

Turnaround Time: 4 to 5 business days

Prenatalsafe® Karyo Plus

Turnaround Time: 5 to 7 business days

Prenatalsafe® COMPLETE

Turnaround Time: 4 to 15 business days

Prenatalsafe® COMPLETE Plus

Turnaround Time: 5 to 15 business days

Prenatalsafe® FULL RISK

Turnaround Time: 5 to 20 business days

All the answers you need for the well-being of your family.

Contact us at
+39 06.164161500 (Contact Center) or fill out this form.

A specialist will contact you, free of charge and without obligation, to provide you with all the information you need.

EXPERIENCE.
COMPETENCE.
QUALITY.

For over 20 years, Eurofins Genoma has been an excellence center in the field of genetics and molecular biology, recognized internationally for its large technological and human resources.

Our laboratories, housed in modern and high-tech facilities, are characterized by advanced instrumental and technological equipment, as well as high-quality standards.

Since 1997 we have mainly operated as a diagnostic partner for genetic, cytogenetic and molecular analysis: we are a research-active company and boast significant knowledge and experience in the field.

We provide a wide range of services among the most complete in the national and international territory, offering patients and their doctors innovative diagnostic solutions for a wide range of genetic and molecular analysis.

Tests performed in Italy

3 laboratories equipped with the most innovative technologies

Quick
reporting

Tests distributed
globally

Over 20 years of experience
in genetics and molecular biology

Over 200,000 genetic tests per year

Personalized genetic counseling

Research department with numerous publications in prestigious international journals

customer service: +39 06.164161500

Rome

Laboratories and Medical Studies

Legal Headquarters and Research and Development Laboratory for Molecular Genetics
Via Castel Giubileo, 11 / 00138

Medical Genetics Laboratory and Molecular Diagnostics

Sampling and Consultations
Via Castel Giubileo, 62 / 00138

Milan

Molecular Genetics Laboratory and Medical Studies

Via Enrico Cialdini, 16 (Affori Centre) 20161

Florence

Laboratory and Medical Studies

Via Cavour, 168r 50121