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Medicover VERAgene NIPT Test

£495.00

Medicover VERAgene NIPT Test

VERAgene NIPT Test and Carrier Screen is the only non-invasive prenatal test (NIPT) that can simultaneously screen for aneuploidies (Down Syndrome, Edward Syndrome, Patau Syndrome) sex chromosome aneuploidy (Turner Syndrome, Kleinfelter Syndrome), microdeletions (22q Deletion or Di George Syndrome) and 100 single gene diseases (Cystic Fibrosis, B-Thalasaemia, Sickle Cell Disease etc). It can also be used to provide basic screening in cases of a vanishing twin.The diseases screened by VERAgene are associated with a moderate to severe health impact  on the health, development and quality of life on the baby. By combining detection of aneuploidies and microdeletions with the screening of monogenic diseases, VERAgene provides a comprehensive solution to prospective parents.

It works for single and twin pregnancies, IVF own egg pregnancies and those with a vanishing twin.

VERAgene needs a maternal blood sample, and a buccal swab sample from the biological father. The maternal blood contains cell-free DNA from both the mother and the fetus. This cell-free DNA is isolated and analyzed along with the father’s DNA sample for any potential genetic mutations using next generation sequencing. Sophisticated bioinformatics algorithms are then used to compute the risk of the fetus having a monogenic disease.

Our fee includes either a FREE ultrasound  scan in our Cardiff Clinic or a FREE home or work phlebotomy blood sample anywhere in the UK or Ireland.

NIPT (Non-Invasive Prenatal Testing) FAQs

What is NIPT?

NIPT (Non-Invasive Prenatal Testing) is a blood test performed during pregnancy that analyses small fragments of fetal DNA circulating in the mother’s blood to screen for certain chromosomal conditions.

What conditions does NIPT screen for?

Most NIPT tests screen for Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18) and Patau syndrome (Trisomy 13). Some expanded panels may also include selected sex chromosome conditions.

When can NIPT be done during pregnancy?

NIPT can usually be performed from 10 weeks of pregnancy onwards. The test involves a simple blood sample from the mother and results are typically available within one to two weeks.

How reliable is NIPT for Down syndrome screening?

NIPT has a very high detection rate for Down syndrome compared with traditional screening tests. However, it is still a screening test rather than a diagnostic test, and positive results are usually confirmed with diagnostic testing.

Can NIPT determine the baby’s sex?

Yes. Most NIPT tests can identify fetal sex by detecting Y-chromosome DNA in the maternal blood sample if parents wish to receive this information.

Why should NIPT be performed through a regulated clinic?

Having NIPT through a HIW-registered clinic ensures that the test is offered with appropriate clinical counselling, safe sample handling and proper follow-up support if results require further investigation.

Click here to learn more about Understanding NIPT in Pregnancy

Click here to learn more about Common Genetic Conditions

Click here to learn more about the VERAgene  100 Single Gene Diseases Panel

Click here to learn about the VeraGene Mutations that are tested

SKU: MCVG Categories: Blood Test, Blood Test, First Trimester, Pregnancy under 24 weeks Tags: Cystic fibrosis, Medicover, monogenic, NIPT, single gene, VERAgene
  • Description

Description

Medicover VERAgene NIPT Test

VERAgene NIPT Test and Carrier Screen  is the only non-invasive prenatal test (NIPT) that can simultaneously screen for aneuploidies (Down Syndrome, Edward Syndrome, Patau Syndrome) sex chromosome aneuploidy (Turner Syndrome, Kleinfelter Syndrome), microdeletions (22q Deletion or Di George Syndrome) and 100 single gene diseases (Cystic Fibrosis, B-Thalasaemia, Sickle Cell Disease etc) . The diseases screened by VERAgene are associated with a moderate to severe health impact  on the health, development and quality of life on the baby. By combining detection of aneuploidies and microdeletions with the screening of monogenic diseases, VERAgene provides a comprehensive solution to prospective parents.

It works for single and twin pregnancies, IVF own egg pregnancies and those with a vanishing twin.

Veragene Pregnancy Types

VERAgene needs a maternal blood sample, and a buccal swab sample from the biological father. The maternal blood contains cell-free DNA from both the mother and the fetus. This cell-free DNA is isolated and analyzed along with the father’s DNA sample for any potential genetic mutations using next generation sequencing. Sophisticated bioinformatics algorithms are then used to compute the risk of the fetus having a monogenic disease.

Click here to learn more about Understanding NIPT in Pregnancy

Conditions are Screened by Veragene
Conditions screened for by Veragene (in pink)

Our fee includes either a complimentary scan in our Cardiff Clinic or a complimentary home or work phlebotomy blood sample anywhere in the UK or Ireland.

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