Getchecked NIPT® – Non-Invasive Prenatal Testing at Getchecked
Get your results within 10 to 15 business days. Getchecked NIPT offers genetic, non-invasive prenatal testing (NIPT) to screen for the most common fetal chromosomal abnormalities. Our test combines the latest next generation sequencing technology with expert medical reporting.
What is the NIPT Test?
The NIPT test, or Non-Invasive Prenatal Testing, is a revolutionary method to screen for genetic conditions in the fetus during pregnancy. In Dubai, the demand for the NIPT test is increasing as more parents seek peace of mind regarding their unborn child's health. The NIPT test in Dubai is a simple blood test that analyzes DNA from the placenta to assess the risk of conditions such as Down syndrome.
Benefits of the NIPT Test in Dubai
One of the main benefits of the NIPT test in Dubai is its high accuracy rate. Compared to traditional screening methods, the NIPT test offers a significantly lower false positive rate, making it a preferred choice among expectant parents. Additionally, the NIPT test in Dubai can be performed as early as the 10th week of pregnancy, allowing for early detection and planning.
How to Get the NIPT Test in Dubai
Getting the NIPT test in Dubai is straightforward. You can consult your healthcare provider, who can refer you to accredited laboratories that offer the NIPT test. Many clinics in Dubai are equipped with state-of-the-art technology to ensure accurate results. Remember to discuss the benefits and limitations of the NIPT test with your doctor before proceeding.
Conclusion
In conclusion, the NIPT test in Dubai is an essential screening option for expectant parents concerned about genetic disorders. With its non-invasive nature and high accuracy, it provides reassurance and critical information for the health of your baby. If you are considering the NIPT test in Dubai, reach out to a healthcare professional to learn more about your options.
Introduction to NIPT Testing
NIPT Testing (Non-Invasive Prenatal Testing) is a cutting-edge screening method that provides expectant parents with crucial information about the health of their unborn child. Unlike traditional methods, NIPT tests are highly accurate and pose no risk to the pregnancy.
What is a NIPT Test?
A NIPT test is a non-invasive prenatal screening test that analyzes small fragments of fetal DNA circulating in a pregnant woman's blood. This test can detect chromosomal abnormalities such as Down syndrome, Edwards syndrome, and Patau syndrome. The NIPT test for pregnancy is typically performed from the 10th week of gestation.
Why Choose NIPT Testing?
- Accuracy: NIPT tests are more accurate than traditional screening methods.
- Safety: Being a non-invasive prenatal screening test, it poses no risk to the fetus.
- Early Detection: NIPT testing can be conducted early in the pregnancy.
NIPT Test in Different Locations
NIPT Test Abu Dhabi
For expectant parents in Abu Dhabi, NIPT testing is available at several top medical facilities. These institutions offer state-of-the-art technology to ensure accurate and reliable results. GetChecked Clinic in Abu Dhabi provides comprehensive NIPT services.
NIPT Test Dubai
Dubai residents can access NIPT testing at numerous healthcare centers known for their excellence in prenatal care. The NIPT test in Dubai is conducted by experienced professionals who ensure a smooth and comfortable experience. Visit GetChecked Clinic in Dubai for trusted NIPT testing.
NIPT Test Sharjah
In Sharjah, NIPT testing is provided by well-reputed clinics that prioritize maternal and fetal health. The NIPT test in Sharjah is accessible and administered with the utmost care. GetChecked Clinic in Sharjah offers reliable NIPT testing services.
How to Prepare for a NIPT Test
- Consult with Your Doctor: Discuss your medical history and any concerns you may have.
- Schedule the Test: Make an appointment at a reliable facility that offers NIPT testing, such as GetChecked Clinic.
- Relax: The NIPT test is non-invasive and involves a simple blood draw.
Internal Links and Further Reading
Conclusion
NIPT testing is a revolutionary approach to prenatal screening, offering expectant parents peace of mind with its accuracy and safety. Whether you are considering a nipt test in Dubai it’s essential to choose a trusted healthcare provider like GetChecked Clinic to ensure the best possible care for you and your baby.
For more detailed information on non-invasive prenatal screening tests and to book your NIPT test for pregnancy, visit our comprehensive resources here.
With Getchecked NIPT Now Offers Non-Invasive Prenatal Testing That Provides a Fast and Accurate Screen for the Most Common Prenatal Chromosomal Abnormalities.*
Getchecked NIPT is performed on a single maternal blood sample and combines the latest next generation sequencing technology with the highest quality medical reporting. It provides unparalleled accuracy and detection compared to other non-invasive testing methods – ultrasonography or nuchal translucency testing.
Why Choose GetcheckedNIPT?
100% SAFE
AS EARLY AS POSSIBLE
FAST & RELIABLE RESULTS
Highly accurate results available within 10-15 business days
EASY HANDLING
Getchecked NIPT kit free of charge. Return shipment via phone call
Expertise You Can Trust
Approximately 1% of All Babies Will Be Born With a Chromosomal Abnormality
- Fetal chromosomal abnormalities are causing physical disability and/or mental retardation
- 70% of syndromic congenital abnormalities are contributed by Trisomy T21, T18 or T13 and 10% by Turner syndrome (Monosomy X)
- The risk of trisomy increases significantly with maternal age
Trisomies
Trisomies
Sensitivity
Specificity
Sex Chromosome Aneuploidies & Fetal Gender
Sex Chromosome Aneuploidies
Concordance with cytogenetic results
GetcheckedNIPT Reporting Information
Getcheked NIPT is only designed to analyze chromosome aneuploidies of the fetus after 10 weeks of gestation. Reported are overrepresentations of chromosomes 21, 18 and 13, as well as the sex chromosome aneuploidies XO, XXX, XXY and XYY. This screening test does not test for aneuploidies in other chromosomes not mentioned above and can therefore not exclude abnormalities in these.
Chromosome aneuploidies for a twin gestation can in general be detected by this test. However, the test cannot be attributed to individual twin fetuses because in twin gestations sensitivity and specificity for detection of aneuploidies are limited. In case of twin pregnancy and detection of only one Y chromosome by the test, the fetal gender of each individual twin cannot be determined by the test.
Getchecked Reports NIPT Results As Follows:
Positive result – if Getchecked NIPT identifies an aneuploidy (chromosome 21, 18, 13 or gonosomal chromosomes), Getchecked NIPT reports presence of aneuploidy and provides data on fetal DNA fraction in the sample of mother´s peripheral blood (in percentages) and the data on fetal gender if requested. We urgently recommend to the referring physician or the genetic counselor to determine and decide if further invasive testing and subsequent analysis is needed.
Negative result – if NIPT did not indicate a trisomy of chromosome 13, 18, or 21 or gonosomal abnormalities, Getchecked Clinic reports a negative result together with the data on fetal DNA fraction and the data on fetal gender if requested. A negative result cannot entirely exclude the possibility of fetoplacental mosaicism. Thus, Getchecked Clinic is giving negative results of NIPT together with the suggestion: if the fetus shows abnormalities on ultrasound investigation, or if a family history of fetal abnormalities or other genetic disorders exists, we urgently recommend to the referring physician or the genetic counselor to determine and decide if further invasive testing and subsequent analysis is needed.
Notion
Sample Preparation and analysis software are CE-IVD marked
Getchecked Clinic's NIPT Is the Earliest and Most Accurate Way To Detect Trisomy 21
Conventional Prenatal Screening Methods vs. GetcheckedNIPT
how it works
Book in Clinic or Home
FDA Approved Laboratory
Personalized Health Plan
Related Packages
Unlock your potential with our curated selection of featured packages
NIPT UNITY Aneuploidy Screen
- Checks for Patau syndrome, caused by an extra chromosome 13.
- Checks for Edwards syndrome, caused by an extra chromosome 18.
- Checks for Down syndrome, caused by an extra chromosome 21.
- Can determine if the baby is a boy or a girl
- Fetal sex, Fetal RhD status, and 22q11.2 deletion syndrome.
Sample Type
- Blood sample from the mother.
Results time 10 - 15 days
UNITY Carrier Screen
- Checks if the mother is a carrier for certain genetic disorders.
- Cystic fibrosis, spinal muscular atrophy, and various other inherited diseases checked by carrier screening.
- Checks the baby's DNA for specific conditions if the mother is found to be a carrier (sgNIPT).
- Drawing a small amount of blood, usually from the mother's arm, to be analyzed in a lab.
Sample Type
- Blood sample from the mother.
Results time 10 - 15 days
UNITY Aneuploidy Screen w/ Fetal Antigen NIPT
- Checks for Patau syndrome, caused by an extra chromosome 13.
- Checks for Edwards syndrome, caused by an extra chromosome 18
- Checks for Down syndrome, caused by an extra chromosome 21.
- Checks for 22q11.2 deletion syndrome, caused by a small missing piece of chromosome 22.
- Checks if the baby has the RhD protein on their red blood cells.
Sample Type
- Blood sample from the mother.
Results time 10 - 15 days
UNITY Complete NIPT+Carrier
- This comprehensive prenatal test combines Carrier Screen and the Aneuploidy Screen.
- Carrier Screen w/ sgNIPT Reflex Aneuploidy Screen w/ T13, T18, T21, and Sex Chromosomes.
- Checks if the mother is a carrier for certain genetic disorders.
- By carrier screening cystic fibrosis, spinal muscular atrophy, and various other inherited diseases are being checked.
Sample Type
- Blood sample from the mother.
Results time 10 - 15 days
UNITY Complete w/ Fetal Antigen NIPT
- Carrier Screen w/ sgNIPT Reflex Aneuploidy Screen w/ T13, T18, T21, and Sex Chromosomes
- Identifies if the mother carries genetic mutations for disorders like cystic fibrosis and spinal muscular atrophy.
- Uses the same blood sample to check the baby's DNA for conditions if the mother is a carrier.
- Detects major chromosomal abnormalities (T13, T18, T21) and sex chromosome issues.
- Determines fetal sex, RhD status, specific red blood cell antigens, and 22q11.2 deletion syndrome.
Sample Type
- Blood sample from the mother.
Results time 10 - 15 days
Basic NIPT for Trisomies 13, 18, 21 & Fetal Sex
- Non-Invasive Prenatal Test (NIPT) using cell-free DNA (cfDNA) from the maternal bloodstream
- Screens for Trisomies 13, 18, and 21, which are associated with significant genetic conditions, providing crucial information about the health of the fetus.
- Detects a wide range of chromosomal abnormalities in the fetus, helping parents and healthcare providers make informed decisions early in the pregnancy.
- Provides detailed information on the fetal chromosomal sex, allowing parents to know the baby’s gender before birth.
Sample Type
- Blood sample from the mother.
Results time 5 - 7 days
NIPT Comprehensive Trisomy, Sex Chromosome, RAA & CNV Test
- The most comprehensive Non-Invasive Prenatal Test (NIPT) tailored for singleton pregnancies, offering thorough screening for Trisomies 13, 18, and 21 to identify major chromosomal abnormalities.
- Includes screening for rare autosomal aneuploidies (RAAs), which are less common chromosomal conditions that could impact the fetus.
- Offers fetal chromosomal sex determination, giving parents the opportunity to find out the baby’s gender early in the pregnancy.
- Detects large copy number variations (CNVs) greater than 7Mb, providing insights into significant structural changes in the chromosomes.
Sample Type
- Blood sample from the mother.
Results time 5 - 7 days
NIPT Miscarriage Analysis & Chromosomal Evaluation
- A Non-Invasive Prenatal Test (NIPT) developed to analyze cell-free fetal DNA following spontaneous pregnancy loss, aimed at identifying underlying genetic abnormalities.
- Screens for chromosomal irregularities that may explain the loss, offering crucial insights into the potential causes.
- Detects significant copy number variations (CNVs) that might reveal structural issues within the chromosomes, providing a clearer understanding of the loss.
- Delivers important genetic data, assisting families with reproductive planning and understanding potential future risks.
Sample Type
- Blood sample from the mother.
Results time 5 - 7 days
Fetal Whole Exome Sequencing
- Sequencing of the entire fetal exome, providing a comprehensive analysis of all coding regions to detect copy number variations (CNVs) and single nucleotide variants (SNVs).
- Identifies genetic alterations in any gene relevant to the analysis, offering a detailed understanding of potential abnormalities.
- Helps detect potential genetic conditions that could impact the fetus, allowing for early diagnosis and informed medical decisions.
- Provides a thorough examination of the fetal genome, ensuring any clinically significant mutations are identified for a more complete genetic evaluation.
Sample Type
- Blood sample from the mother.
Results time 14 - 30 days
Whole Exome Sequencing (WES) Screening
- Comprehensive genetic screening for newborns, analyzing over 390 genetic conditions that may impact early development and health.
- Provides early detection of genetic conditions, offering valuable insights for preventive care and management.
- Enables early interventions and personalized care plans, helping to mitigate potential health issues before they arise.
- Offers a proactive approach to newborn health, enhancing the ability to manage genetic conditions from the start of life.
Sample Type
- Blood sample from the mother.
Results time 14 - 30 days
BabyPeek
Available for free as an add-on to all UNITY Packages.
- Includes: Traits: Eye color, Red hair, Curly hair, Light or dark hair, Hair thickness, Freckles, Cilantro, Bitter taste, Asparagus odor, Sweet taste, Sweet vs. salty, Teeth
Sample Type
- Blood sample from the mother.
Results time 10 - 15 days
