Objective:
- Risk-free screening for chromosomal abnormalities at the earliest possible time in pregnancy

The Non-Invasive Prenatal Test (NIPT) involves an examination of the mother’s blood. It is suitable as a risk-free alternative to placenta puncture as well as amniocentesis. In this test, the cell-free, fragmented DNA of the child, which enters the maternal bloodstream in small quantities, is analyzed in the mother’s venous blood. The results provide information on whether Down syndrome (trisomy 21) is present with a reliability of more than 99 percent. The detection rate is 92 percent for trisomy 13 and 96 percent for trisomy 18. The test is performed in combination with an ultrasound examination. If the NIPT is performed early (11th week of pregnancy), the first quarter ultrasound including preeclampsia screening is recommended in the 12th – 14th week of pregnancy.
- The results are available approx. 5-10 working days after the examination.
Corona safety measures
The highest possible Corona safety standards are our top priority. Therefore, we request that you come to the Prenatal Center only for an agreed appointment. One companion is welcome.
Invoicing and payment
After the respective examination you will receive an invoice. You can pay us by debit or credit card at your convenience.
Your ultrasound images are immediately available to you digitally
A special EDP program makes it possible to transmit the ultrasound images and video sequences to a cell phone number or an Email address of your choice by means of a secure link. Thus, if you wish, you can get the images immediately on your smartphone.
Information on twin pregnancies
Even though twin pregnancies usually proceed without major complications, they are classified as high-risk pregnancies from a medical perspective. We have compiled information on possible risks and tips for expectant mothers of twins.
Forms and information sheets
You can download forms and information sheets here.
CONSULTATION / EXAMINATION | FEE |
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Early Screening | EUR 150,- |
Screening 12 – Extended Combined Test | EUR 250,- (for multiples: EUR 300,-) |
Screening 22 – Organ screening | EUR 250,- (for multiples: EUR 300,-) As a follow-up examination: EUR 200,- (for multiples: EUR 250,-) |
Screening 32 – Wellbeing ultrasound with Doppler examination | EUR 200,- (for multiples: EUR 250,-) As a follow-up examination: EUR 150,- (for multiples: EUR 200,-) |
Cervical ultrasound (included in the organ screening) | EUR 80,- |
3D ultrasound | EUR 200,- |
Ultrasound package in case of medical necessity of repeated growth checks (e.g. diabetes, previous illnesses of the expectant mother) | Depending on requirements |
The non-invasive prenatal test (NIPT) can also be booked as a 2-part examination. In this variant, from the 10+0 week of gestation, the blood sample for the NIPT is combined with a short ultrasound examination, and from the 12+0 week of gestation, the neck fold measurement and the first trimester screening are carried out. The costs specified below increase by EUR 50,- with this procedure (EUR 100,- in the case of a twin pregnancy). |
|
NIPT Mini Non-Invasive Prenatal Test | Testing for trisomy 21: EUR 300,- + associated ultrasound examination including preeclampsia screening: EUR 250,- |
NIPT Classic Non-Invasive Prenatal Test | Testing for trisomy 21, 18 and 13: EUR 600,- On request, gender determination + associated ultrasound examination including preeclampsia screening: EUR 250,- |
NIPT Extended Non-Invasive Prenatal Test | Testing for trisomy 21, 18 and 13 Testing for sex chromosomes and rare microdeletions: EUR 800,- On request, gender determination + associated ultrasound examination including preeclampsia screening: EUR 250,- |
NIPT Spezial Non-Invasive Prenatal Test | Testing for monogenic diseases such as mucoviscidosis (cystic fibrosis), spinal muscle diseases, sickle cell disease, thalassemia: EUR 800,- + associated ultrasound examination including preeclampsia screening: EUR 250,- |
NIPT Rhesus Non-Invasive Prenatal Test | Determination of the child's Rhesus factor: EUR 300,- (no ultrasound examination required) |
Chorionic Villus Sampling | EUR 600,- |
Amniocentesis | EUR 600,- |
Genetic counseling | EUR 150,- |
COMBINATION TARIFFS |
|
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Screening 12 + Screening 22 | EUR 450,- (for multiples: EUR 500,-) |
Screening 12 + Screening 22 + Screening 32 | EUR 600,- (for multiples: EUR 650,-) |
The costs for the above-mentioned examinations are not covered by the statutory health insurance.