We understand and want to reach every mother who has years to bond deeper with the tiny heart forming and beating inside of her. Panorama is a market-leading non-invasive prenatal screening test (NIPT) that reveals your baby’s risk for genetic disorders as early as 9 weeks. New nurturing research has shown that a passionate bond or a connection between a mother and her infant may help forestall sicknesses, support invulnerability, and improve a baby’s IQ. This is what we try to achieve through fetal Genetic testing. Our NIPT blood test Service in Keighley will take you one step closer to connecting with the little flutters in your belly. An ultrasound scan is offered for Only viability (heartbeat) and gestation measurements for people who have not had an early scan with the NHS and don’t know how many weeks pregnant.
Panorama NIPT analyzes a baby’s (placental) DNA through a simple blood draw from the mother’s arm and gives you a fulfilling result. Miracle Inside Diagnostic Centre near Huddersfield offers a variety of genetic blood tests during pregnancy to interpret genetic risks involved in the pregnancy.
Panorama Postal NIPT Test
Please Contact us for more information to know about these NIPT Postal blood test Kits, please call 📞 01138301371 to speak with the Healthcare Professional. If you choose PANORAMA Non-Invasive Prenatal Testing, The package will include:
An early viability or growth scan (scan selection will depend on your stage in pregnancy)
The opportunity to discuss your results with an experienced Genetic counselor about early pregnancy genetic testing and the Consultation will have expert advice.
Information about various options and assist with your choices
- Standard Panorama NIPT blood test without ultrasound scan – £400.00
- Standard Panorama NIPT blood test with ultrasound scan – £450.00 ( a Quick Viability Scan is offered till 15 weeks of Pregnancy )
Screens for T21, T18, and T13, 22q11.2 deletion syndrome (DiGeorge), sex chromosome. NIPT blood test is also available for Twin pregnancies.
Pre-test and Post-test counseling are conducted for better guidance about genetic blood testing during pregnancy. ( If required)
Blood samples are then collected by the courier on the same day
Results are available to you within 7-10 days.
To Book a Panorama NIPT Blood test with Ultrasound Scan, please Click BOOK NOW.
- Panorama NIPT blood test including 5 micro-deletions without ultrasound scan – £450.00
- Panorama NIPT blood Test including 5 micro-deletions £500
– Panorama + 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.
– Blood samples are collected by the courier on the same day. Pre-test and Post-test counseling are conducted for better guidance. ( If required)
– Panorama extended microdeletion panel: add 1p36, Angelman, Cri-du-chat, Prader-Willi
– Optional fetal sex, with 100% accuracy.
– It is applicable to twin pregnancies, egg donors, and surrogate pregnancies.
– We will detect vanishing twins (the first source of false positives with other tests), report individual fetal fractions, give individual fetal sex, and report chorionicity at 9 weeks.
We provide a same-day blood result service for some blood tests (Monday – Friday, excluding Bank Holidays). A £ 25 for Phlebotomy + Courier charge will be applied for all Bloods . Please inform us at the time of booking if you require same-day results.
To Book Panorama with Microdelitios NIPT Blood test with Ultrasound Scan, please Click BOOK NOW.
Panorama Test – Learn more
Information on Test Specifications
PANORAMA NIPT Blood Test – An Overview
Panorama NIPT is the only non-invasive prenatal screening test that distinguishes between fetal and maternal cell-free DNA. The credit goes to the SNP-based sequencing and Natera’s proprietary algorithm. Using advanced bioinformatics techniques, Panorama screens for a broad range of chromosomal conditions, including:
- Chromosome Abnormalities
- Trisomy 21 (Down syndrome)
- Trisomy 18 (Edwards syndrome)
- Trisomy 13 (Patau syndrome)
- Triploidy
- Sex Chromosome Abnormalities
- Monosomy X (Turner syndrome)
- Klinefelter syndrome
- Triple X syndrome
- XYY syndrome
Microdeletions
- 2 deletion syndrome
- 1p36 deletion syndrome
- Prader Willi syndrome
- Angelman syndrome
- Cri-du-chat syndrome
- Gender of the Baby (optional)
In Twin Pregnancies
Non-identical or fraternal twins
- Trisomy 21 (Down syndrome)
- Trisomy 18 (Edwards syndrome)
- Trisomy 13 (Patau syndrome)
- Gender of each twin (optional)
Moreover, if our screening finds that your twins are identical, Panorama can additionally screen for:
- Monosomy X (Turner syndrome)
- Sex chromosome trisomies
- 2 deletion syndrome (optional)
- Egg Donor or Surrogate Pregnancies
- Trisomy 21 (Down syndrome)
- Trisomy 18 (Edwards syndrome)
- Trisomy 13 (Patau syndrome)
- Gender (optional)
According to the International Society for Prenatal Diagnosis (ISPD) and American College of Medical Genetics and Genomics (ACMG) support offering NIPT as a first-line screen, non-invasive prenatal testing is appropriate as a Primary Screening Test for pregnant women of all ages. Down Syndrome and certain other chromosomal conditions occur more frequently in babies born to mothers over 35 years old. Other conditions for which NIPT screens – such as microdeletion syndromes – occur with the same frequency in babies, regardless of the mother’s age.
https://www.natera.com/panorama-test
Contact us for more information to know about these NIPT blood tests with Ultrasound, please call 📞 01138301371 to speak with the Healthcare Professional.
Vistara Test ( Prenatal Test additional to Panorama Test)
Go beyond chromosomal anomalies and assess single-gene disorders.
Identifying single-gene mutations is usually done after childbirth or during childhood. However, due to the evolution of NIPT, Vistara NIPT, a prenatal DNA test goes beyond detecting chromosomal conditions to assess single-gene disorders. Vistara -Single Gene NIPT does not test for chromosomal abnormalities such as extra chromosomes (Trisomy) or test for your baby’s gender. It is done to identify single-gene mutations that affect your baby’s health. Miracle Inside Diagnostic Centre located near Otley provides Vistara prenatal tests addition to panorama test for just £850
Secure your spot in the best Non-Invasive Prenatal DNA testing
When should you take it? From 9 weeks of Pregnancy
What is the turnaround time ? 2 to 3 weeks
Vistara -Single Gene NIPT test – An Overview – £850
Vistara is a NIPT blood test performed to find small DNA changes or single-gene mutations which might affect a baby’s health. Like every other NIPT prenatal screening blood test, a blood sample is taken from the mother’s arm to analyze DNA from the placenta found in the blood.
Vistara is a simple blood test and can be performed as early as nine weeks of pregnancy. Vistara, a fetal genetic testing method screens for serious conditions across 30 skeletal, cardiac and neurological disorders with a combined incidence of 1 in 600 – Noonan syndrome, Achondroplasia, Osteogenesis, Imperfecta, Rett syndrome, Craniosynostosis.
To Book now your Vistara ( Pre-natal Test additional to Panorama Test) in Leeds Click Here
Miracle Inside at Harrogate offers the best Vistara Prenatal Test addition to the Panorama test which
- screens serious genetic conditions caused by single-gene mutations across 30 genes which affects the quality of life and may benefit from medical and/or surgical intervention
- screens for a set of genetic disorders that, combined, occur more frequently than Down Syndrome
- screens Genetic conditions that are not tested by traditional NIPTs or carrier screening
- Vistara -Single Gene NIPT does not have any risk of miscarriage.
Opt for a Vistara -Single Gene NIPT blood test for the following indications:
- Paternal age (over 40 years)
- If you’d like to know as much as possible or as an extra to your Panorama Test, CVS, or amniocentesis
- If ultrasound anomalies are identified on your scan (such as shortened long bones, increased NT measurements, or cardiac defects)
The focus here is on de novo dominant disorders, at the SNP level. This is useful for advanced paternal age (35+) and non-specific ultrasound findings such as shorter long bones. For each condition, the attached list has the lists of genes we analyze, the detection rates, types of ultrasound findings, and clinical actions.
Please Click here to Download the Vistara Patient Brochure
To speak to our healthcare professional to know more about these blood tests, call 📞 01138301371.
Check the following website for more information: