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NIPT

PrenatalSAFE® 3 - £400

PrenatalSAFE® is a Non-Invasive Prenatal test which, by analysing the free circulating fetal DNA isolated from a sample of maternal blood, provides 6 levels of information in Pregnancy. The test allows for the detection of aneuploidies and microdeletion syndromes, from the most common to the rarest, structural alterations in all the chromosomes of the fetus and the presence of mutations related to serious genetic diseases.

PrenatalSAFE® 3 – £ 400 

For screening of aneuploidies such as Downs, Edwards, Patau, Turner, Jacobs  with a  Dating Ultrasound Scan Included 

  • 30 minute Appointment with Qualified Health Professional
  • 1 samples of blood taken from arm of mother
  • Optional DNA sexing of Baby Optional Extra (singleton pregnancy only)
  • Results of test emailed to client
PrenatalSAFE® 5 – £ 500

PrenatalSAFE® 5 – £ 500 

For screening of aneuploidies such as Downs, Edwards, Patau, Turner, Jacobs and Klinefelter Syndromes, plus Trisomy X with a  Dating ultrasound scan

  • 30 minute Appointment with Qualified Health Professional
  • 1 samples of blood taken from arm of mother
  • with this package is Included DNA sexing of Baby (singleton pregnancy only)
  • Results of test emailed to client
PrenatalSafe KARYO – £ 1250

PrenatalSAFE KARYO – £ 1250 

Screens all the conditions included in PrenatalSafe 5, plus less frequent chromosomal aneuploidies such as Trisomy’s 1 to 22. 

  • 30 minute Appointment with Qualified Health Professional
  • 1 samples of blood taken from arm of mother
  • with this package is Included DNA sexing of Baby (singleton pregnancy only)
  • Results of test emailed to client
PrenatalSafe KARYO PLUS – £ 1500

PrenatalSAFE KARYO PLUS – £ 1250 

Analyses every chromosome in the genome as well as 9 clinically significant microdeletion syndromes DiGeorge, Cri-du-chat, Prader-Willi, Angel man, 1p36 deletion, Wolf-Hirschhom, Jacobsen, Langer-Giedion, Smith-Magenis Syndromes.

  • 30 minute Appointment with Qualified Health Professional
  • 1 samples of blood taken from arm of mother
  • with this package is Included DNA sexing of Baby (singleton pregnancy only)
  • Results of test emailed to client

 For More details please  Visit http://www.prenatalsafe.co.uk/ for more informations

GENESAFE™ Inherited  - £ 1000

Genesafe Facilitates Early Diagnosis Of Single-Gene Disorders. The First Non-Invasive Prenatal Test That Screens Multiple Genes For Mutations Causing Severe Genetic Disorders In The Foetus From £1000

GeneSafe works as a complementary screen to traditional and genome-wide NIPT PrenatalSafe KARYO. GeneSafe screens for several life-altering genetic disorders that are not screened with current NIPT technology, allowing for a more complete picture of the risk of a pregnancy being affected by a genetic disorder.

All pregnant women regardless of age are at equal risk of the genetic conditions screened by GeneSafe. Although the occurrence of each disorder is relatively rare, the cumulative rate of these conditions (~1 to 600) is similar to that of Down Syndrome, in younger women.

GeneSafe is broken down into 3 different levels of screening:

GeneSafe ™ INHERITED – £ 1000

  • This test screens for 5 common inherited recessive genetic disorders, such as Cystic Fibrosis, Beta-Thalassemia, Sickle cell anemia, Deafness autosomal recessive type 1a and 1b.
  • Allows detection of common inherited disorders within the foetus.
  • Genes screened: CFTR, CX26 (GJB2), CX30 (GJB6), HBB
GeneSafe ™ De Novo – £ 1000

GeneSafe ™ De Novo – £ 1000

  • This test screens for 44 severe genetic disorders due to de novo mutations (a gene mutation that is not inherited) in 25 genes. 
  • Many disorders screened with GeneSafe De Novo are not typically associated with abnormal prenatal ultrasound findings (especially in the first trimester), or may not be evident until late second/third trimester, when confirmatory invasive testing can pose a risk of pre-term birth, or baby’s health after delivery.
  • Genes screened: ASXL1, BRAF, CBL, CHD7, COL1A1, COL1A2 , COL2A1, FGFR2, FGFR3, HDAC8, JAG1, KRAS, MAP2K1, MAP2K2, MECP2, NIPBL, NRAS, NSD1, PTPN11, RAF1, RIT1, SETBP1, SHOC2, SIX3, SOS1
GeneSafe™ Complete – £ 1500

GeneSafe Complete – £ 1500

  • This test screens for both inherited and de novo single-gene disorders and represents a combination of the tests GeneSafe Inherited and GeneSafe De Novo providing a complete picture of the pregnancy risk. 

For More details please  Visit  https://www.genesafe.co.uk/  for more informations

Special Offer


  • We are offering as  a  Introductory  offer  both  GENESAFE  COMPLETE  test   and  PRENATALSAFE KARYO PLUS  together for  £ 2700   ( as  opposed  to  £ 3000 ).
  • Call us  today on  01132008760 to take advantage of  this Amazing Special  Offer.

 

HOW IT WORKS   - PROCEDURE FOR THE TEST

  • BOOK   the test in from 10 weeks with Mircale Inside 3D/4D Baby Scan Centre
  • COMPLETE  the Test Request and Consent Form on the Day
  • PROVIDE   1 Blood Sample  
  • RECEIVE   the Results within  4- 5 working days*

PRENATALSAFE  test  is a non-invasive prenatal test (NIPT) that offers the reassurance of knowing in the early stages of pregnancy, as early as 10 weeks, that your baby is at low risk of Down Syndrome (Trisomy 21), Edwards Syndrome (Trisomy 18), and Patau Syndrome (Trisomy 13). Other tests that are commonly requested are sex chromosome linked conditions such as Klinefelter syndrome and Turner syndrome. (Please discuss with your healthcare provider to suggest if these are right for you). The NIPT test does not assess risk for mosaicism, partial trisomies or translocations. The test will provide accurate answers when they matter most—simply, safely, sooner.

2. How is it carried out?

Your baby’s cell free DNA can be detected circulating in your blood and so it requires a simple blood test, which is then sent to GENOMA Genetic’s labs , analysed and the results returned within 1 week. You will also be required to have an ultrasound scan prior to the blood test to check the viability of your pregnancy.

3. Who can have the Genesis Serenity prenatal test?

It can be carried out for most pregnancies. Including IVF, singleton and twins. It can be performed on women who conceived via assisted reproductive technology (ART), including use of a donor egg.

4. Is the NIPT test conclusive?

Although it’s not 100% conclusive, PRENATALSAFE  test is highly accurate. The NIPT  test identifies in singleton pregnancies more than 99% of fetuses with Trisomy 21, 98% of fetuses with Trisomy 18, and 98% of fetuses with Trisomy 13, and 95% of fetuses with Turner Syndrome. X and Y analysis provides >99% accuracy for fetal sex. Accuracy for detecting other sex chromosome anomalies varies by condition. The risk of requiring further testing such as CVS or Amniocentesis after a PRENATALSAFE  NIPT is dramatically reduced.

5. How does NIPT test differ from NHS tests?

The PRENATALSAFE   test is able to deliver a much higher accuracy than NHS tests giving you greater peace of mind. It’s totally non-invasive, posing minimal risk to mother or baby, can test for more than just Down Syndrome and can be carried out as early as 10 weeks pregnant. NHS Down Syndrome screening tests are typically undertaken via a nuchal translucency ultrasound between 11 and 14 weeks. NIPT test can only estimate the risk of your baby having Down’s, it can’t tell you for sure either way. For example, if your result is one in 1,000, this means that for every 1,000 babies with your level of risk, one will have Down’s syndrome. A risk of one in 150 or less is considered high. If for some reason the scan cannot be completed, expectant mothers are offered a blood test between 14 and 20 weeks of pregnancy, which is less accurate than the nuchal test. Further testing such as CVS and amniocentesis are invasive and have risk factors associated with them.

6. How does the PRENATALSAFE  test differ from other NIPTs on the market?

Our laboratory is based in SPAIN , ensuring that your results are returned to you faster than many of our competitors who send blood samples to the United States or China for analysis.

7. Where can I get the Best NIPT test in Leeds?

Miracle Inside 3D/4D Baby Scan Centre offer the PRENATALSAFE  test at its clinics in Leeds , Ls102Bd . To make an appointment call 01132008760 during office hours or email admin@miracleinside.com

8. How long does it take?

Once you have seen your Healthcare Professional and had your scan then a simple blood sample is taken from the expectant mothers arm to be sent to  Eurofins labs for processing which will take less than 1 week. Results are sent to the healthcare professional to forward to patients.

9. NIPT Test Clinics

To make an appointment at our clinics please call our customer services team on 01132008760 during office hours or email admin@miracleinside.com

10ADVANTAGES OF THE PRENATALSAFE 

  • IT'S SIMPLE
  • IT'S RELIABLE - 99.9% sensitivity for chromosomes 21,18 13 and aneuploidy of sex chromosomes with a false positive rate lower than 0.01%. (Fiorentino et Al., 2016)
  • IT'S SAFE  - It is a non-invasive test, no risk to the fetus or the mother.
  • IT'S SENSITIVE - It allows detecting chromosomal aneuploidies even at low quantities of fetal DNA (2%), unlike other tests that require a quantity of fetal DNA> 4%.
  • IT'S QUICK - Thanks to the new high-resolution FAST technology, the PrenatalSAFE test results will be available from 3 working days.
  • IT'S CLEAR  -  PrenatalSAFE® is the non-invasive prenatal test that provides the clearest results: aneuploidy DETECTED or aneuploidy NOT-DETECTED, within the limits of resolution of the method
  • Free follow-up of abnormal results
  • Reimbursement of the test fee for cases with inconclusive test results
  • Free RhSafe test for pregnant women Rh(D) negative with husband Rh(D) positive
  • Pre and Post-test genetic counselling 

Gestational age of the PrenatalSafe- Please ensure you will be at least 10 weeks pregnant at the time of your scheduled appointment NIPT Test in Yorkshire.

For More details please  Visit  https://www.genesafe.co.uk/,http://www.prenatalsafe.co.uk/ , https://www.prenatalsafekaryo.co.uk/  for more information’s about NIPT

 

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