Prenatal package - promo price
NIPTiva (non-invasive prenatal testing) represents the most advanced method of prenatal screening, allowing for the early detection of the most common chromosomal abnormalities in a baby from a simple maternal blood sample. Thanks to modern laboratory processes and automated sample processing, results are available quickly, with a high level of accuracy and reliability.
Why choose NIPT?
- High result accuracy with a 99% rate
- Completely safe for mother and fetus
- Early testing starting from the 10th week of pregnancy
- Fast results within 5 to 7 working days
- Reduces the need for invasive diagnostic procedures
- Analysis based on state-of-the-art Illumina technology
Who is the non-invasive prenatal test recommended for?
NIPTiva is recommended for all pregnant women who want additional reassurance and information about their baby's health, and especially:
- Pregnant women over 30 years of age
- Pregnant women with a twin pregnancy
- Pregnant women who have had spontaneous miscarriages
- Pregnant women who conceived through IVF
- Pregnant women with a family history of genetic disorders
- Pregnant women who want a non-invasive and reliable prenatal assessment
- Pregnant women who received abnormal results from a double/triple test or ultrasound
When is the right time for testing?
NIPT can be done as early as the 10th week of pregnancy, when the amount of fetal DNA in the mother's blood is sufficient for high-quality analysis. Early testing allows you to receive important information in a timely manner and provides additional peace of mind during pregnancy.
What does the process look like?
- Blood draw at Primea Polyclinic (no special preparation needed; you can eat and drink normally before the test)
- Sample analysis 5–7 working days
- Test results and medical consultation
At Primea, NIPTiva packages are available with an included 20% discount:
NIPTiva Basic Twins Package
A non-invasive prenatal test for singleton and twin pregnancies that covers the basic trisomies (T21, T18, T13).
What the test covers:
- Down syndrome (trisomy 21)
- Edwards syndrome (trisomy 18)
- Patau syndrome (trisomy 13)
NIPTiva Twins Package
An extended non-invasive prenatal test for twin and singleton pregnancies which, in addition to basic trisomies, provides insight into structural changes on all chromosomes and reveals the baby's sex.
What the test covers:
- Down syndrome (trisomy 21)
- Edwards syndrome (trisomy 18)
- Patau syndrome (trisomy 13)
- Aneuploidies of all chromosomes (1–22)
- Trisomies and monosomies of all chromosomes (1–22)
- Microdeletions, deletions, and duplications of all chromosomes larger than 7Mb
- Sex information
NIPTiva Gold Package
A comprehensive test that, in addition to the three most common trisomies, analyzes abnormalities in the number of sex chromosomes, providing important early information about your baby's health and sex.
What the test covers:
- Down syndrome (trisomy 21)
- Edwards syndrome (trisomy 18)
- Patau syndrome (trisomy 13)
- Sex chromosome aneuploidies:
- Turner syndrome (monosomy X)
- Klinefelter syndrome (XXY trisomy)
- Triple X syndrome (trisomy X)
- Jacobs syndrome (XYY trisomy)
- Sex information
NIPTiva Platinum Package
An advanced package that combines the analysis of the most common trisomies, sex chromosome aneuploidies, and the detection of large structural chromosomal changes (microdeletions and deletions) for greater peace of mind during pregnancy.
What the test covers:
- Down syndrome (trisomy 21)
- Edwards syndrome (trisomy 18)
- Patau syndrome (trisomy 13)
- Sex chromosome aneuploidies:
- Turner syndrome (monosomy X)
- Klinefelter syndrome (XXY trisomy)
- Triple X syndrome (trisomy X)
- Jacobs syndrome (XYY trisomy)
- Microdeletions, deletions, and duplications of all chromosomes larger than 7Mb
- Sex information
NIPTiva Diamond Package
A premium prenatal test that provides complete insight into the baby's genome. It covers all autosomal chromosomes (from 1 to 22), sex chromosomes, as well as microdeletions, providing the maximum available screening for chromosomal abnormalities.
What the test covers:
- Down syndrome (trisomy 21)
- Edwards syndrome (trisomy 18)
- Patau syndrome (trisomy 13)
- Sex chromosome aneuploidies:
- Turner syndrome (monosomy X)
- Klinefelter syndrome (XXY trisomy)
- Triple X syndrome (trisomy X)
- Jacobs syndrome (XYY trisomy)
- Aneuploidies of all chromosomes (1–22)
- Trisomies and monosomies of all chromosomes (1–22)
- Microdeletions, deletions, and duplications of all chromosomes larger than 7Mb
- Sex information
NIPTiva Brilliant Package
The most comprehensive non-invasive prenatal test on the market. In addition to a complete analysis of all chromosomes and microdeletions, this package includes screening for the most common single-gene (monogenic) disorders, providing parents with absolute peace of mind.
What the test covers:
- Down syndrome (trisomy 21)
- Edwards syndrome (trisomy 18)
- Patau syndrome (trisomy 13)
- Sex chromosome aneuploidies:
- Turner syndrome (monosomy X)
- Klinefelter syndrome (XXY trisomy)
- Triple X syndrome (trisomy X)
- Jacobs syndrome (XYY trisomy)
- Aneuploidies of all chromosomes (1–22)
- Trisomies and monosomies of all chromosomes (1–22)
- Microdeletions, deletions, and duplications of all chromosomes larger than 7Mb
- Sex information
- Screening for monogenic disorders:
- Cystic fibrosis
- Spinal muscular atrophy (SMA)
- Wilson's disease
- Gilbert's syndrome
- Duchenne muscular dystrophy
Why the combination of the NIPTiva test with a gynecological ultrasound exam is the best choice
By combining a modern NIPTiva test and an expert gynecological ultrasound exam, expecting parents gain a comprehensive insight into the course of the pregnancy and the baby's development. While NIPTiva provides information about the risk of certain chromosomal abnormalities, an ultrasound exam allows for the assessment of the fetus's anatomical development and pregnancy monitoring.
This complementary combination provides significant support in pregnancy monitoring and making informed decisions during prenatal care.
