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PrenatalSAFE®

is a non-invasive and risk free test

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PrenatalSAFE®

meets every need: 6 levels of depth

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PrenatalSAFE®

detects aneuploidies, structural chromosomal abnormalities and genetic disorders

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Call the Toll-free Number 800 501 651 (working only in Italy)
or send us an email to info@prenatalsafe.it

One of our specialists will contact you, for free and with no obligation, to provide you with all the information you need. CONTACT US

What is PrenatalSAFE® test ?

PrenatalSAFE® is a non-invasive prenatal test that, analyzing circulating cell-free fetal DNA isolated from a sample of maternal blood, and includes 6 levels of depth thanks to which is possible to achieve the most complete pregnancy informational framework available today. In fact, the test allows seeing aneuploidies and microdeletion syndromes, from the most common to the rarest, structural abnormalities in all fetus chromosomes and the presence of mutations related to severe genetic disorders.

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It's Easy

A simple blood sample (8-10 ml) collected at 10^ weeks of gestation is required, from which the circulating cell-free fetal DNA is analyzed.

It's Safe

It is a non-invasive test, therefore the risks of abortion present in traditional invasive prenatal diagnosis techniques, such as amniocentesis and CVS, are eliminated. No risk for the fetus and the mother.

It's Fast

Thanks to the new high resolution FAST Technology, PrenatalSAFE turnaround time is just of 3 working days.

It's reliable

99,9% sensibility for chromosomes 21, 18, 13, and sex chromosomes aneuploidies with a percentage of false positives lower than 0.01 ( Fiorentino et Al., 2016)

It's sensitive

It allows detecting chromosome aneuploidies even at small quantities of fetal DNA (2%), unlike other tests that require a quantity of fetal DNA > 4%..

Clear results

PrenatalSAFE® is the non-invasive prenatal test that provides the clearest results: aneuploidy DETECTED or NO aneuploidy DETECTED, within the limits of the resolution of the method.

 

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The step by step procedure

Step1. Order the test
Order the test asking for the blood sample transport container
Step.2 Perform blood sampling
Prepare the blood tubes for shipping by following the instructions.
Step3. Fill in the set of forms
Fill in the set of forms (informed consent, registration form, etc.).
Step4. Sample shipping
Send samples to our laboratory using the transport container
Step5. Genetic consultation
Invite the patient to book genetic counseling at our Center
Step6. Analysis Results
In about 3-7 working days from sample receipt you will receive the result of the PrenatalSAFE® test

THE MOST INNOVATIVE AND COMPLETE “MADE IN ITALY” PRENATAL TEST"

PrenatalSAFE® is the most innovative and complete non-invasive prenatal test on fetal DNA in maternal blood available today, and is performed entirely in ITALY at GENOMA Group laboratories.

No level of investigation of PrenatalSAFE® tests is sent in service to laboratories located abroad.


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Indication

Who can undergo PrenatalSAFE® test

PrenatalSAFE® examination is the best test in the following cases:

• Pregnancies in which invasive prenatal diagnosis is contraindicated (ex. Risk of spontaneous abortion)
• Positive first trimester screening (Bi-Test)
• Advanced maternal age (> 35 years)
• Advanced paternal age (> 40 years)
• Positivity to first or second trimester screening tests
• The ultrasound scan shows fetal abnormalities, suggesting aneuploidy
• Personal/familial anamnesis of chromosomal abnormalities
• Partner(s) carrier of balanced Robertsonian translocation of chromosomes 13 or 21.
• Couples with advanced paternal age (PrenatalSAFE® COMPLETE)

All the pregnant women of at least 10 weeks of gestation can perform the test.

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our numbers

Reliability without comparisons

%
SENSITIVITY AND SPECIFICITY OF THE TEST
DAYS TO RECEIVE THE REPORT
PROFESSIONALS AT YOUR SERVICE
YEARS OF EXPERIENCE IN THE FIELD

6 Levels of in-depth analysis

PrenatalSAFE® test types available
Non-invasive prenatal test for the identification in pregnancy of the most common fetal aneuploidies. The test detects the presence of aneuploidies 13, 18 and 21, X and Y, and 6 deletion syndromes.
Non-invasive prenatal test for the identification in pregnancy of fetal aneuploidies and structural abnormalities on every chromosome of the fetal karyotype, and of 9 microdeletion syndromes.
Non-invasive prenatal test for the identification in pregnancy of fetal aneuploidies and structural abnormalities on every chromosome of the fetal karyotype, the identification of mutations responsible of severe genetic disorders both hereditary or de novo, and of 9 microdeletion syndromes.

RELIABILITY OF PRENATALSAFE® TEST

99,9% sensibility for chromosomes 21, 18 and 13 and aneuploidies of sex chromosomes with a false positive percentage lower than 0,1%. ( Fiorentino et Al., 2016)

  • Trisomy 21
    %
  • Trisomy 18
    %
  • Trisomy 13
    %
  • SCA
    %

FREE SERVICES OFFERED BY OUR CENTER

Find out all the benefits.
GENETIC COUNSELLING

PRE-TEST AND POST-TEST GENETIC COUNSELLING

In order to explain to patients the aims of the analysis, the achievable results and those emerged upon completion of the exam.

FAST Procedure

FAST Procedure

Thanks to the recent introduction of the new high-resolution FAST Technology, the exam results will be available after only 3-5 working days.

RhSafe® Test

RhSafe® Test

Non-invasive prenatal exam that allows determining the fetal Rh(D) Factor. The RhSafe® test is optional and is performed for free (upon request) in Rh(D) negative pregnant women.

FREE FOLLOW-UP OF ABNORMAL RESULTS

FREE FOLLOW-UP OF ABNORMAL RESULTS

Chorionic villus sampling or Amniocentesis free at reference gynecologists affiliated with Genoma. Free follow-up of abnormal result in case of positive outcome for aneuploidy, structural chromosomal abnormality or presence of genetic mutation.

SAMPLES COLLECTION AND TRANSPORT KIT

SAMPLES COLLECTION AND TRANSPORT KIT

Certification in accordance with UN3373 and free shipping service of biological samples at our laboratories.

ALL INCLUSIVE CUSTOMER SERVICE

ALL INCLUSIVE CUSTOMER SERVICE

From the sample shipping to the reporting, information on collection methods and samples conservation.

SCIENTIFIC AND SPECIALISTIC SUPPORT

SCIENTIFIC AND SPECIALISTIC SUPPORT

Molecular biologists and qualified geneticists are always available to assist clients in interpreting results.

Educational

Educational

GENOMA provides its clients the informative material for Doctors and information brochures for patient.

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