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 8 levels of depth thanks to which is possible to achieve the most complete pregnancy informational framework available today. In fact, the test allows detecting 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.

PrenatalSAFE® is offered by the Genoma Group laboratories in Milan and Rome and is available in eight versions, each with a different depth level, in detail:


PrenatalSAFE Full Risk
Combines PrenatalSAFE® Karyo Plus + GeneSafe™ Complete with GeneScreen® FOCUS, a carrier screening test for both parents to identify mutations in genes linked to the most common, and potentially transmissible, recessive inherited diseases in Italy.


PrenatalSAFE Complete Plus
Analyzes all chromosomes in the fetal genome, identifying chromosomal aneuploidies, structural aberrations (i.e., deletions and duplications) of 7 Mb, 9 microdeletion syndromes, and severe genetic disorders in the fetus.



Through the analysis of circulating cell-free fetal DNA (cfDNA) in maternal blood, it screens for fetal karyotype and severe genetic disorders in the fetus.



It screens for aneuploidies and structural chromosomal abnormalities (deletions or segmental duplications) across the fetal genome.



Moreover allows detecting the presence in the fetus of 9 of the most common microdeletion syndromes.

structural chromosomal alterations


It screens for Trisomy 21, Trisomy 18, Trisomy 13, sex chromosomes (X and Y) aneuploidies and includes the determination of fetal gender (optional).



In addition to PrenatalSAFE® 5 test, it also provides the option of a further analysis to detect trisomy 9 and 16 and the presence of structural chromosomal alterations, that is 6 of the most common microdeletion syndromes.

structural chromosomal alterations


It screens for Trisomy 21, Trisomy 18, Trisomy 13 and includes the determination of fetal gender (optional).


We remember you that
PrenatalSAFE® can be integrated with RhSafe® test, a non-invasive prenatal exam that, by analyzing the fetal DNA isolated from a blood sample of the pregnant woman, allows determining Rh(D) fetal Factor. The RhSafe® test is optional, and is performed for free (on request) in Rh(D) negative pregnant women with a Rh(D) positive male partner.

 
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