Non-Invasive Prenatal Testing
NIPT offers expectant parents the latest in antenatal screening technology, to estimate a risk of a baby being born with a genetic condition. 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.
TRIMESTER ONE©
This NIPT test solely screens for Down's syndrome. For a deeper understanding of Downs syndrome please visit the NHS website or gain further support from The Downs Syndrome Association
Downs Syndrome (Trisomy 21)
Gender Determination (optional)
Available from 9 Weeks
TRIMESTER 2©
Trimester 2 screens for Downs syndrome, Patau’s syndrome and Edwards syndrome. Also screened are the genetic conditions Klinefelter syndrome, Jacobs syndrome and Trisomy X that are solely linked with sex 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
Optional Gender Determination
Available from 10 Weeks
TRIMESTER 3©
Trimester 3 screens for all the genetic conditions in Trimester 2, plus the trisomy of chromosomes 9 and 16. The test also detects the presence of the 6 most common micro-deletion syndromes.
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
Plus 6 Microdeletion Syndromes
Di George Syndrome
Cri du Chat Syndrome
Angelman Syndrome
Wolf-Hirschorn Syndrome
1p36 Deletion Syndrome
Prader-Willi Syndrome
TRIMESTER 4©
Trimester 4 tests for all the genetic conditions in Trimester 3 plus screening a more extensive profile of genetic condition for those who wish to for a wider screening test of serious conditions affecting; motor skills, physical features, speech and language, and causing distinctive behavioural problems.
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
Plus 9 Microdeletion Syndromes
Di George Syndrome
Cri du Chat Syndrome
Angelman Syndrome
Wolf-Hirschorn Syndrome
1p36 Deletion Syndrome
Prader-Willi Syndrome
Langer Giedion Syndrome
Jacobsen Syndrome
Smith-Magenis Syndrome
TRIMESTER COMPLETE GENETIC©
Trimester Complete is the most technologically advanced non-invasive prenatal screening test currently available. Screening for all conditions included within Trimester 4, plus inherited and non-inherited conditions to give an extensive genetic screening profile.
Also testing the fathers genetic profile, Trimester Complete is usually taken by those who wish to have comprehensive genetic screening during pregnancy.
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
Plus Inherited & Non-Inherited including:
Noonan Syndromes
Deafness Type 1A
Deafness Type 1B
Thalassaemia
Sickle Cell Anaemia
Skeletal Disorders
Craniocynostosis Syndrome
Syndromatic Disorders
Plus 9 Microdeletion Syndromes
Di George Syndrome
Cri du Chat Syndrome
Angelman Syndrome
Wolf-Hirschorn Syndrome
1p36 Deletion Syndrome
Prader-Willi Syndrome
Langer Giedion Syndrome
Jacobsen Syndrome
Smith-Magenis Syndrome
Here for you.
Available now at one of our nationwide clinics or in the comfort of your own home.
We Go the Extra Mile
If you are unsure which is the the best method of antenatal screening for you discuss it with your midwife or obstetrician or simply book a consultation with us. All Trimester non-invasive pre-natal screening tests are collected by courier and processed in UKAS accredited laboratories in Europe. Unlike other tests on the market, Trimester NIPT tests are not outsourced to external laboratories in the US or China.
Pre-Consultation
Book a pre-test consultation to decide which test is right for you.
Blood Test
Attend one of our clinics, or in the comfort of your own home.
Results
+ Interpretation, dedication clinical lead will talk you through your test results.