Non Invasive Prenatal (NIPT) Test £325 onwards

Non-Invasive Prenatal Testing (NIPT)

Gain valuable insights of your fetus genetic conditions as early as 10 weeks with NIPT

NIPT is a sensitive screening blood test that can be taken as early as 10 weeks of pregnancy to detect Downs, Edwards' & Patau's syndrome. Miracle Inside, a Private genetic blood test center located near Wakefield, aims at providing safe and accurate . NIPT blood tests to assess the chromosomal anomalies of the fetus at an early stage. A ultrasound scan  is offered for Only viability (heartbeat) and gestation measurements for people who have not had a early scan with the NHS and dont know how many weeks pregnant .

Our NIPT Blood test Centre near Halifax, now offers the following NIPT tests such as Veracity NIPT, Panorama NIPT, Harmony NIPT, Prenatalsafe NIPT.

Reserve your spot now for the best NIPT test in Yorkshire at £325

How early can you take the NIPT test?        From 10 weeks of pregnancy

How long will it take?                                     15-30 Minutes.

An Overview of Non-Invasive Prenatal Testing:

The most recent breakthroughs of fetal genetic testing is NIPT which analyses cell-free maternal and fetal DNA in the mother's blood. Non-Invasive Prenatal Testing (NIPT) is a form of genetic testing during pregnancy that provides insights about the genetic conditions of your fetus. In this test, blood is drawn from the mother's arm and sent to the laboratory to extract and analyse cell-free DNA material. 

NIPT is not a diagnostic test but it is a screening test for chromosomal abnormalities like Downs , Edwards' & Patau's syndrome. However, large-scale studies show that the test has a 99% detection rate for Down’s Syndrome. Though it is not reliable Edwards' syndrome and Patau's syndrome, it can look for these two conditions.

In addition to our range of Ultrasound Baby scan services, we also offer the following NIPT test at our Miracle Inside 3D 4D Baby Scanning Centre near  Keighley.

VERACITY  Option 1  without Scan - £ 325

VERACITY  Option 1 with Scan - £ 350

  • Trisomy 21: Down syndrome
  • Trisomy 18: Edwards syndrome
  • Trisomy 13: Patau syndrome
  • A ultrasound scan  is offered for Only viability (heartbeat) and gestation measurements for people who have not had a early scan with the NHS and dont know how many weeks pregnant .

To Book Veracity Option 1, please Click   BOOK NOW

 

VERACITY  Option 2 without ultrasound Scan  - £ 375

VERACITY  Option 2 with Ultrasound Scan  - £ 400

  • Trisomy 21: Down syndrome
  • Trisomy 18: Edwards syndrome
  • Trisomy 13: Patau syndrome
  • Aneuploidies* X, Y ( Monosomy X - Turner syndrome: X0, Triple X syndrome: XXX, Klinefelter syndrome: XXY, Jacobs syndrome: XYY, XXYY syndrome )
  • Fetal Gender detection is Complimentary
  • A ultrasound scan  is offered for Only viability (heartbeat) and gestation measurements for people who have not had a early scan with the NHS and dont know how many weeks pregnant .

To Book VERACITY Option 2, please Click   BOOK NOW  

HARMONY  Prenatal Test - £ 400

  • Trisomy 21: Down syndrome
  • Trisomy 18: Edwards syndrome
  • Trisomy 13: Patau syndrome
  • The Harmony Test is primarily used for the detection of Trisomy 21,18 and 13, however, you can request X and Y analysis providing over 99% accuracy for your baby’s gender. This option is also available for twin pregnancies.
  • Sex Chromosome conditions - ( Optional extra ) The Harmony test can also assess the risk of sex chromosome conditions XXX, XYY, XXYY, XXY, and a missing X chromosome in a girl (Turner Syndrome) A female fetus with a single X chromosome. These babies have a high risk of miscarriage and heart problems.
  • 22q11 deletion Screening - ( Optional extra )TDL Genetics is now offering 22q11.2 deletion screening as an additional optional Extra in the Harmony prenatal test menu. 22q11.2 deletion is the underlying cause of conditions described as DiGeorge Syndrome and velocardiofacial syndrome (VCFS). This option will be discussed at your appointment to determine whether requesting this is right for you.
  • A ultrasound scan  is offered for Only viability (heartbeat) and gestation measurements for people who have not had a early scan with the NHS and dont know how many weeks pregnant .

To Book Harmony Prenatal Test, please Click   BOOK NOW

The IONA® Screening Test - £400

  • Trisomy 21: Down syndrome
  • Trisomy 18: Edwards syndrome
  • Trisomy 13: Patau syndrome
  • A ultrasound scan  is offered for Only viability (heartbeat) and gestation measurements for people who have not had a early scan with the NHS and dont know how many weeks pregnant .

The IONA® test is a safe non-invasive and accurate screening test for Downs Syndrome, Edwards’ Syndrome, and Patau’s Syndrome.  We can take this test comfortably at your home to anyone who had a scan to date the pregnancy. The ideal time is around 10 weeks. The test is more accurate than the standard combined test offered by the NHS as it uses DNA from the baby found in the mother’s blood to assess risk.

To Book IONA® Screening Test, please Click   BOOK NOW

PANORAMA  Non-Invasive Prenatal Test  - £480.00

  • Trisomy 21: Down syndrome
  • Trisomy 18: Edwards syndrome
  • Trisomy 13: Patau syndrome
  • A ultrasound scan  is offered for Only viability (heartbeat) and gestation measurements for people who have not had a early scan with the NHS and dont know how many weeks pregnant .
  • Panorama is a market-leading non-invasive prenatal screening test (NIPT) that reveals your baby’s risk for genetic disorders as early as nine weeks. Panorama analyzes a baby's (placental) DNA through simple blood drawn from the mother’s arm.
  • Screens for Trisomy 21, Trisomy 18 and Trisomy 13 , 22q11.2 deletion syndrome (DiGeorge), sex chromosome. Available even for Twin pregnancies
  • Pre-test and Post-test counselling.

To Book Panorama NIPT Test, please Click   BOOK NOW

VERACITY Option 3  without Ultrasound scan  -  £475

VERACITY Option 3  with Ultrasound scan  -  £ 500

  • Trisomy 21: Down syndrome
  • Trisomy 18: Edwards syndrome
  • Trisomy 13: Patau syndrome
  • Aneuploidies* X, Y ( Monosomy X - Turner syndrome: X0, Triple X syndrome: XXX, Klinefelter syndrome: XXY, Jacobs syndrome: XYY, XXYY syndrome )
  • Microdeletions ( DiGeorge syndrome - 22q11.2 deletion, 1p36 deletion syndrome , Smith-Magenis syndrome - 17p11.2 deletion , Wolf-Hirschhorn syndrome - 4p deletion )
  • Fetal Gender detection is Complimentary
  • A ultrasound scan  is offered for Only viability (heartbeat) and gestation measurements for people who have not had a early scan with the NHS and dont know how many weeks pregnant .

To Book Veracity Option 3, please Click   BOOK NOW

PANORAMA  Non-Invasive Prenatal Test including 5 micro-deletions -   £560.00

  • Panorama Test  + 5 microdeletions screens for T21, T18, T13 , Sex chromosome, Triploidy, Monosomy X, Di George Syndrome, 1p36 deletion syndrome, Angelman syndrome, Prader-Willi syndrome and Cri-du-chat syndrome.
  • An ultrasound is included.
  • Pre-test and Post-test counselling

To Book Panorama NIPT Test, please Click   BOOK NOW

VERAgene Comprehensive NIPT  -  £850

  • Trisomy 21: Down syndrome
  • Trisomy 18: Edwards syndrome
  • Trisomy 13: Patau syndrome
  • Aneuploidies* X, Y ( Monosomy X - Turner syndrome: X0, Triple X syndrome: XXX, Klinefelter syndrome: XXY, Jacobs syndrome: XYY, XXYY syndrome )
  • Microdeletions ( DiGeorge syndrome - 22q11.2 deletion , 1p36 deletion syndrome , Smith-Magenis syndrome - 17p11.2 deletion , Wolf-Hirschhorn syndrome - 4p deletion )
  • Monogenic disorders (100 monogenic disorders such as Cystic Fibrosis, Gaucher disease,
    Canavan disease; please see the brochure for the list of disorders, by clicking complete list of monogenic conditions screened )
  • Fetal Gender detection is Complimentary
  • A ultrasound scan  is offered for Only viability (heartbeat) and gestation measurements for people who have not had a early scan with the NHS and dont know how many weeks pregnant .

To Book VERAgene Comprehensive NIPT, please Click   BOOK NOW

Vistara ( Prenatal Test additional to Panorama Test) - £850

Vistara NIPT does not test for chromosomal abnormalities such as extra chromosomes (eh, Down's syndrome ) or test for your baby's gender. Vistara test screens small DNA changes, or single-gene mutations, which will affect your fetus's health. It helps in detecting on de novo dominant disorders, at the SNP level, which includes Noonan and Rett syndrome, achondroplasia, osteogenesis imperfecta, craniosynostosis, etc.

To Book Vistara Test, please Click   BOOK NOW 

 

For More Information CLICK HERE

To know more information about these blood tests speak to our Healthcare Professional, call us on 📞 01138301371

The following websites might provide further useful information regarding your NIPT blood tests,

https://www.arc-uk.org/

https://www.harmonytest.co.uk/

https://www.arc-uk.org/tests-explained/downs-syndrome-screening

Please note

  • We will require details of your GP / Health Care Professional, which may be requested prior to or at the time of the scan.
  • This scan requires access to the area of interest, therefore it is recommended to wear loose clothing to facilitate this process.
  • Blood results require interpretation and All results should be shared with your regular healthcare professional / GP / Fertility specialist.
  • All of our first line ultrasound scans & health Blood tests are optional. You must be at least 16 years old and you should have no existing medical condition or treatment pending that relates to the scan/blood test you are booking. If you are in any doubt about having any type of test, you should consult your GP.
  • The Geneticist, in the context of Genetic Counselling, will explain in detail the test result and advise to confirm the result by invasive prenatal diagnosis. is provided as part of some of these Blood test Services. Customers regular Healthcare professional / GP / Fertility specialist is responsible for ensuring appropriate counselling provided to the patient.
  • Please note: £100 non-refundable deposit is payable upon booking. Should you wish to alter your appointment time; please give the boutique a minimum of 48 hours notice. 

Frequently Asked Questions

What are Down syndrome, Edwards syndrome, and Patau syndrome?

Down syndrome, Edwards syndrome, and Patau syndrome are genetic disorders caused by chromosomal trisomies.

Down syndrome is caused by an additional copy of chromosome 21. It is characterized by intellectual impairments and congenital anomalies. Down syndrome occurs roughly in 1 in 700 births but is most common in women over 35 years of age.

Edwards syndrome is caused by an extra copy of chromosome 18, and Patau syndrome is caused by an additional copy of chromosome 13. Edwards syndrome and Patau syndrome occur less common of about 1 in 3000 and 1 in 10000 pregnancies, respectively. Edwards and Patau syndromes are characterized by severe congenital abnormalities and rarely survive past the first year of life.

What are sex chromosome aneuploidies?

Sex chromosome aneuploidies are genetic diseases caused by the presence or absence of a sex chromosome. The 23rd pair of chromosomes determines the sex of an individual. Women have XX chromosomes and men have XY chromosomes.

There are four major sex chromosome aneuploidies:

  • Turner syndrome is characterized by the presence of a single X chromosome.
  • Triple X syndrome is characterized by the presence of three X chromosomes.
  • Klinefelter syndrome is characterized by the presence of two X chromosomes and one Y chromosome.
  • Jacob syndrome is characterized by the presence of one X chromosome and two Y chromosomes.

What are microdeletions?

Microdeletions are genetic conditions in which part of a chromosome will be lost. Microdeletions are characterized by congenital abnormalities and intellectual impairment. The severity of the symptoms varies depending on the size and location of the microdeletion. The most common microdeletion syndrome is DiGeorge syndrome which occurs approximately once in 1000 pregnancies. The prevalence of DiGeorge syndrome increases to 1 in 100 in pregnancies with major structural anomalies such as congenital heart disease.

Additional Information:

  • Please ensure that you are at least 10 weeks pregnant at the time of your scheduled appointment for early pregnancy genetic testing at Miracle Inside
  • It is advisable to keep your body well hydrated and warm prior to your appointment as it may affect the ability to take blood samples sometimes.
  • NIPT can not be done for multiple gestation pregnancies with 3 or more fetuses. It is also not recommended for pregnant women with a history of bone marrow transplantation or other illnesses. For more clarification, please contact us.
  • We will require details of your GP / Health Care Professional, which may be requested prior to or at the time of the scan.
  • This scan requires access to the area of interest, therefore it is recommended to wear loose clothing to facilitate this process.
  • Blood results require interpretation and All results should be shared with your regular healthcare professional / GP / Fertility specialist.
  • All of our first line ultrasound scans & health Blood tests are optional. You must be at least 16 years old and you should have no existing medical condition or treatment pending that relates to the scan/blood test you are booking. If you are in any doubt about having any type of test, you should consult your GP.
  • The Geneticist, in the context of Genetic Counselling, will explain in detail the test result and advise to confirm the result by invasive prenatal diagnosis. is provided as part of some of these Blood test Services. Customers regular Healthcare professional / GP / Fertility specialist is responsible for ensuring appropriate counselling provided to the patient.

REFUND:

  • £50 non-refundable deposit is payable upon booking.
  • If you wish to change your appointment schedule, you should give notice before 48 hours of your original date.

Book now to reserve your spot for NIPT Test Leeds

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