A highly accurate and safe pre-natal blood test, available now in the UK. Can be taken from week 10 of pregnancy.

The PrenatalSAFE 5 NIPT blood test is a comprehensive, non-invasive test for expectant mothers to check for the main health conditions that can affect your baby. It also includes gender identification to tell you the sex of you baby or babies – from only 10 weeks of pregnancy.

This prenatal blood test checks traces of the baby’s DNA in your blood for:

• Down Syndrome (Trisomy 21)
• Edwards Syndrome (Trisomy 18)
• Patau Syndrome (Trisomy 13)
• Turner Syndrome (Monosomy X)
• Klinefelter syndrome
• Jacobs Syndrome
• Gender Identification – single pregnancies and identical twins

These tests are more comprehensive than those offered on the NHS to high risk mothers, and can be taken by any expectant mother, regardless of risk status.

Suitable from 10 weeks pregnancy onwards, and for all single pregnancies.

Free post-test genetic counselling is provided for any results which show a positive chance of a condition affecting your baby or babies.

Analysed in a leading UK laboratory, the test is suitable for all pregnant women from 10 weeks of pregnancy onwards, with single or multiple foetuses and conceived naturally or using IVF/Donor Eggs. You do not have to be considered high risk, and can be of any age to take this test.

Based on an internal study from Eurofins Genoma, the test is highly accurate, with positive predictive values (the likelihood of the result being correct and not a false-positive) of:

• Trisomy 21 (Down Syndrome) – 99.32%
• Trisomy 18 (Edwards Syndrome) – 98.94%
• Trisomy 13 (Patau Syndrome) – 82.22%
• Monosomy X or Turner Syndrome (sex chromosome disorder) – 80%
• Klinefelter syndrome (sex chromosome disorder) – 94.44%
• Jacobs Syndrome (sex chromosome disorder) – 96.30%

Unlike an invasive test such as an Amniocentesis, this simple blood test does not pose any risks to a pregnant woman or her unborn child. It is the safest way to detect genetic health conditions before birth.

What are Sex Chromosome Disorders?

Our test includes a check for sex chromosome aneuploidies, common types of sex chromosome disorders. Sex chromosome aneuploidies refer to conditions in which an individual’s sex chromosomes are abnormal in number. Normally, a person has two sex chromosomes, either two X chromosomes (female) or one X and one Y chromosome (male). However, in sex chromosome aneuploidies, there is an extra or missing sex chromosome, leading to various physical and developmental abnormalities.

For example, some common sex chromosome aneuploidies include Turner syndrome (or Monosomy X), which results from a missing X chromosome in females, and Klinefelter syndrome, which results from an extra X chromosome in males. These conditions can affect physical features, such as height and fertility, as well as cognitive and behavioural development.

When will I get the results?

The results will be sent to you directly in 5-7 days of the sample being received at the laboratory. The results report will clearly state whether the conditions have been detected so you can take this information to your GP for further discussion and investigation if needed.

Free post-test genetic counselling is provided for any results which show a positive chance of a condition affecting your baby or babies.