PrenatalSafe 5 + Di George Syndrome

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)
• Sex Chromosomes - X & Y
• Di – George Syndrome
• Gender Determination (optional) 

This test provides analysis of chromosomes 13, 18, 21, the sex chromosomes Turners Syndrome (Monosomy X), Jacobs Syndrome (Trisomy XYY), Trisomy X  and Klinefelter Syndrome (Trisomy XXY) find out more about sex chromosomes. Plus 22q 11deletion syndrome. Find out more about Di George Syndrome

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 10 Working Days. Processed in the EU.