Service

NIPTIFY whole-genome test

NIPTIFY whole-genome NIPT test

A non-invasive prenatal test using a sample of the mother’s blood. From as early as week 10 of pregnancy, it assesses the most common chromosomal changes in the baby with high accuracy — with no risk to the baby.

  • Just a blood test from a vein — safe for mother and baby
  • Possible from week 10 of pregnancy
  • Trisomy 21 (Down syndrome), 18 and 13
  • Whole-genome analysis — other chromosomal changes too
  • Baby’s sex, if you wish
320 €
/ test

From week 10 of pregnancy · No special preparation needed

What happens at the visit

How the test works

01

Consultation: we discuss your stage of pregnancy and what the test shows.

02

A blood sample is taken from a vein — it takes a few minutes.

03

Explaining the results and, if needed, drawing up a plan for next steps.

Dr. Karina Ozola, gynaecologist

This service is provided by

Dr. Karina Ozola

Certified gynaecologist, obstetrician and ultrasound specialist. Sees patients from the age of 14.

Frequently asked questions

No, it complements screening. If the test shows an increased risk, your doctor will recommend a confirmatory test.

No, no special preparation is needed.

We will tell you the exact turnaround time when you book the test.

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