Routine NHS screening takes place between 12 and 14 weeks Many families opt for NIPT testing as it can be taken as early as 10 weeks and, is a more detailed and complementary screening tool for many genetic disorders that are not routinely analysed with current NHS technology.
NIPT provides you with a clearer picture of the risk of your pregnancy being affected by a chromosome abnormality or single genetic disorder.
What's Included?
- Downs Syndrome (Trisomy 21)
- Patau’s Syndrome (Trisomy 13)
- Edwards Syndrome (Trisomy 18)
- X & Y
- Gender Determination (optional)
This test provides analysis of chromosomes 13, 18, 21 and includes analysis of the X and Y sex chromosomes. Find out more about sex chromosomes
This test is suitable for single and *twin pregnancies.
*Only the presence or absence of the Y chromosome can be reported in twins.
Results from 3 Working Days. Processed within the UK.
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