£305.00

Prenatal test to identify genetic conditions in unborn babies, early screening for the three most common chromosomal conditions.

  • Can be performed from 10 weeks into pregnancy
  • 100% safe for mum and baby – only a blood sample from mum required
  • Tests for Down’s Syndrome, Edward’s Syndrome and Patau’s Syndrome
  • Uses next-generation sequencing to analyse foetal DNA and detect chromosomal abnormalities

Please note: This test is not suitable for anyone carrying more than two foetuses, or for dichorionic twins (where there are two placentas present).

Please complete the information below before purchasing this test.

Product total
Options total
Grand total

Description

Test from as early as 10 weeks into pregnancy (10 weeks gestation).

You must have this confirmed via an ultrasound scan before your blood sample is collected to ensure you are at least 10 weeks pregnant, and the blood collection for your NIPT test should be arranged within 1 week of the scan – this is to ensure the most accurate dating of your pregnancy when the test is carried out.

You can choose to have an ultrasound scan via a private provider, or during your routine pregnancy check-ups via the NHS.

Bloods must be taken by a qualified professional , Doctor, Nurse or  Phlebotomist – Contact us if you need help with this.

– you may also attend our head office in Greater Manchester for a blood draw free of charge.

Reviews

There are no reviews yet.

Be the first to review “Non‑invasive Prenatal Genetic Test (NIPT)”

Your email address will not be published. Required fields are marked *