What is neoBona?
neoBona is the most advanced non-invasive prenatal genetic screening test on the market that detects the most frequent chromosomal abnormalities in pregnancy: Down syndrome (trisomy 21), Edwards syndrome (trisomy 18) and Patau syndrome (trisomy 13) together with alterations in the sex chromosomes.
Is this test suitable for me?
neoBona IS INDICATED FOR THE FOLLOWING CASES:
- Is available from 10 weeks of pregnancy (10 weeks + 0 days)
- Can be performed in cases of assisted reproduction, including IVF after gametes donation
- Is suitable for twin pregnancies
- Is a genetic screening test and, as such, must be prescribed by your physician
Why choose neoBona?
AVAILABLE OPTIONS
neoBona is a new generation NIPT test that provides highly reliable results for the screening of:
- Most common chromosomal abnormalities1 (21, 18 y 13)
- Sex chromosome abnormalities and fetal gender
neoBona GenomeWide provides the most complete view of the fetal genome analysing all 23 pairs of chromosomes to expand screening to other rare chromosomal2 abnormalities by assessing the presence of:
- Abnormalities in the remaining autosomes (non-sex chromosomes)
- Partial deletions and duplications3, CNVs of size greater than or equal to 7 Mb on all autosome
1 Alteration in the number of copies of a chromosome.
2 These anomalies could be of clinical relevance as they are associated with miscarriages, various structural alterations, fetal anomalies and developmental and/or growth delays of the fetus.
3 Partial losses or gains of chromosomal regions.
SINGLE PREGNANCY
- Trisomies 21, 18 and 13
- Fetal sex (optional)
- Aneuploidies sex chromosomes + fetal sex (optional)
TWIN PREGNANCIES
- Trisomies 21, 18 and 13
- Determination of the presence of Y chromosome (optional)
RESULTS
MAXIMUM 5 WORKING DAYS
SINGLE PREGNANCY
- Trisomies 21, 18 and 13
- Fetal sex (optional)
- Aneuploidies sex chromosomes + fetal sex
- On all autosomal chromosomes (non-sex chromosomes):
- Aneuploidies
- Duplications/deletions (CNVs) greater than or equal to 7 Mb in size
TWIN PREGNANCIES
- Trisomies 21, 18 and 13
- Determination of the presence of Y chromosome
- On all autosomal chromosomes (non-sex chromosomes):
- Aneuploidies
- Duplications/deletions (CNVs) greater than or equal to 7 Mb in size
RESULTS
MAXIMUM 5 WORKING DAYS
For all types of pregnancies: one/two fetuses, IVF, donation, vanishing or non-evolving foetus.