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NON INVASIVE PRENATAL TESTING

NIPT is regarded as gold standard testing and used to identify the risk of genetic conditions during pregnancy.

NIPT is performed using a simple blood test from the mother with no risk to your unborn baby in comparison to one of the 'next step' diagnostic tests such as Amniocentesis or Corionic Villus Sampling. Each test is performed using a simple maternal blood sample at one of our recommended clinics or at home. 

 

NIPT is recommended in genetic medicine because it offers expectant parents the latest in antenatal screening technology.

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PLEASE PHONE US IN ORDER TO MAKE A NIPT BOOKING - BOOKINGS FOR THIS SERVICE CANNOT BE TAKEN ONLINE.

NIPT TEST TWO

£475

This test provides analysis of chromosomes 13, 18, 21 and X and Y sex chromosomes.

  • Downs Syndrome (Trisomy 21)

  • Patau’s Syndrome (Trisomy 13) 

  • Edwards Syndrome (Trisomy 18)

  • X & Y

  • Gender Determination (optional)  

  • Available from 10 Weeks

  • Results within 3-5 Working Days

NIPT TEST THREE

£695

This test gives you valuable information about the chromosomal status of the growing baby and screens all 24 chromosomes for the most common conditions, this includes analysis of chromosomes 9 and 16 which are known to cause intellectual and physical abnormalities and miscarriage.


Newer tests take advantage of next-generation sequencing (NGS) to bring a Whole Genome Sequencing(WGS) approach to NIPT, expanding test options beyond chromosomes 21, 18, and 13 to include rare autosomal aneuploidies (RAAs), sex chromosome aneuploidies (SCAs), and partial deletions and duplications

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  • All 24 Chromosomes 

  • Downs Syndrome (Trisomy 21)

  • Patau’s Syndrome (Trisomy 13) 

  • Edwards Syndrome (Trisomy 18)

  • Turners Syndrome (Monosomy X)

  • Klinefelter Syndrome Trisomy XXY)

  • Jacobs Syndrome (Trisomy XYY)

  • Trisomy X​

  • Gender Determination (optional) 

  • Available from 10 weeks

  • Results within 3-5 Working Days​

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