GENETIC SCREENING DURING PREGNANCY
GenePlanet NIPT
With a single blood test, you can learn about the most important genetic characteristics without any risk to the fetus. One of the cornerstones of a conscious, prepared pregnancy is to be able to make decisions in a timely manner with reliable information.
WHAT IS THIS TEST?
What a single study reveals
During pregnancy, a small amount of the fetus's genetic material can be detected in your blood. This is what NIPT (non-invasive prenatal test) is based on: it provides information about the probability of the most common chromosomal abnormalities - such as Down's, Edwards' and Patau's syndromes - without invasive intervention and fetal risk, from a single simple blood test.
HEALTH & RISK ASSESSMENT
Why is it worth doing a genetic test?
We offer the test in collaboration with GenePlanet, a genetic laboratory with an international background, because:
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Accredited, EU laboratory background
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with strict quality and data protection standards
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Wide range of filters
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with expandable packages on demand
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Extensive clinical experience
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with background knowledge of tens of thousands of completed tests
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International professional recognition
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recommended by gynecological specialists in several countries
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In case of high risk
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free confirmation test at our partner institution
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THINGS TO KNOW
What you should know about the test
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Highly reliable: screens for the most common trisomies with a sensitivity of over 99%
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Can be performed from the 10th week of pregnancy
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It can be recommended for any pregnant woman, regardless of age or previous risk assessment.
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Can also be used in cases of twin pregnancy, in vitro fertilization (IVF), donor egg pregnancy and previous recurrent miscarriage
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There is no risk to the fetus as it is made exclusively from your blood
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Combined with nuchal fold measurement, it gives an even more accurate picture
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Its reliability is supported by extensive international clinical trials
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The test also determines the sex of the fetus.
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Results are available within 6–10, and in the case of the extended (Mono) test within 15–17 working days.
WHAT DOES THE TEST ANSWER?
All 46 chromosomes of the fetus
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Numerical differences
when only one (monosomy) or three (trisomy) copies of a chromosome are present instead of the usual pair; the most common are T21 (Down), T18 (Edwards) and T13 (Patau)
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Structural differences
the absence (deletion) or duplication (duplication) of a chromosome segment
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Single gene variations
conditions caused by a single gene variant, typically non-heritable mutations that appear for the first time in the fetus (can be tested as part of the Premium package)
Types of NIPT genetic tests
Types of genetic tests
Basic
Down, Edwards, Patau syndrome + gender determination
130,000 HUF
MyAncestry
+ sex chromosome aneuploidies (Turner, Klinefelter, Triple X, Jacobs) + 9/16/22 and other trisomies/monosomies
152,000 HUF
Pro
+ 92 microdeletion syndromes (e.g. DiGeorge) and additional microdeletions/duplications
220,000 HUF
Premium
+ 218 single gene mutations (Mono) tested
496,000 HUF
Twins Basic
Twin pregnancy — basic trisomy screening
152,000 HUF
Twins Pro
Twin pregnancy — extended screening
195,000 HUF
The results of genetic tests are for informational purposes only and are not a substitute for medical diagnosis or treatment.
You can learn more about the exact sampling process and purchasing the package by email, in person, or during an online consultation.
Types of genetic tests
CF & SMA Carrier
It shows whether you carry the gene variants responsible for cystic fibrosis or spinal muscular atrophy (SMA). These conditions can only be passed on to a child if both parents carry the given variant. Requested with NIPT: 89,000 HUF.
49,000 HUF
NIPT Rh
In RhD-negative pregnant women, it determines the RhD blood group status of the fetus, thus avoiding unnecessary prophylaxis against D antibody.
50,000 HUF
The results of genetic tests are for informational purposes only and are not a substitute for medical diagnosis or treatment.
You can learn more about the exact sampling process and purchasing the package by email, in person, or during an online consultation.
Please note that genetic tests can only be taken in person !