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neoBona GenomeWide

690.00€ VAT included

neoBona detects the most frequent chromosomal anomalies in pregnancy through the study of the free DNA of the fetus present in the maternal blood, being the most complete and reliable test on the market.

Descripción

ABOUT THE TEST

Chromosomal abnormalities, like trisomy 21 (Down's syndrome), are present in the 1-2% of the fetuses.

neoBona is a non-invasive prenatal test (NIPT) that detects chromosomal abnormalities in the fetus without any risk to the future baby, providing highly reliable results for the screening of:

  • Aneuploidies1 most common chromosomes (21, 18 y 13)
  • Aneuploidies of the sex chromosomes and fetal sex
1Alteration in the number of copies of a chromosome.

neoBona GenomeWide provides a more complete view of the fetal genome by analyzing los 23 chromosome pairs to expand screening to other rare chromosomal abnormalities2 when evaluating the presence of:

  • Anomalies in the rest of the autosomes (non sex chromosomes)
  • Deletions and partial duplications3, CNVs of size greater than or equal to 7 Mb in all autosomes
2These anomalies could have clinical relevance as they are associated with pregnancy loss., various structural alterations, fetal abnormalities and developmental and/or growth delays of the fetus.
3 Losses or partial gains of chromosomal regions.

Conventional first trimester screening consists of an analysis and an ultrasound, and provides a statistical risk index. neoBona GenomeWide directly analyzes free fetal DNA, which provides greater reliability and a better detection rate, along with fewer false positives.

The sensitivity of conventional screening is 90%, This means that of each 100 fetuses with Down syndrome (trisomy 21), 10 would not be detected (false negatives). The overall sensitivity of neoBona GenomeWide is greater than 99% for Down syndromes, Edwards and Patau (trisomies 21, 18 y 13).

Unlike other prenatal tests, neoBona GenomeWide analyzes free fetal DNA through a technology that allows determining the size of free DNA fragments, improving the reliability of the result.

IS IT RIGHT FOR ME?

neoBona GenomeWide is indicated for the following cases:

  • From the 10th week gestation (10 weeks + 0 days)
  • It can be done in cases of rassisted production, including IVF with gamete donation
  • It is suitable for twin pregnancies
  • It is a genetic screening test and as such must be prescribed by a doctor

PRELIMINARY CONSIDERATIONS

  • It is necessary to go to a SYNLAB center to take the test
  • It is not necessary to go on an empty stomach
  • Necessary medical prescription

WHAT IS THE PROCEDURE?

The test requires a blood sample, so You need to go to a SYNLAB center to take the test so follow the next steps!

  1. Find your nearest center here: SYNLAB CENTERS
  2. go to the center the day you prefer the pide quotes ASK FOR A DATE
  3. the day of your visit, go to the center with your printed invoice or on your mobile and show your DNI or passport
  4. Your results will be available in 5 Work days

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neoBona

465.00€ VAT included

neoBona detects the most frequent chromosomal abnormalities in pregnancy through the study of the free DNA of the fetus present in the maternal blood, being the most complete and reliable test on the market.

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