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Our Non Invasive Prenatal Test offers expecting parents a reliable, comprehensive screening for potential genetic disorders. Gain insights into your baby’s health and confidently plan your pregnancy journey.
Test at our network labs across Thailand or via Clinician Assisted Lab Draw at your On-Demand Location*
✅ Non-invasive prenatal testing, as simple as a blood test
✅ Up to 99% accurate results in a short timeframe
✅ Safe for both mother and baby
✅ Early Detection (as early as 10 weeks)
✅ Endorsed by leading medical experts and ISO 15189 certified
Open Daily 8am-10pm. 2 Minutes Walk from BTS Nana, BTS Asok and MRT Sukhumvit.
*Get your test at home or hotel for an extra 750 baht only, a clinician can be at your location within 1 to 3 hours.
Please find a detailed description of our available packages below
Available for single pregnancy only. For twin pregnancy, see NIPT Twin package.
Available for single pregnancy only. For twin pregnancy, see NIPT Twin package.
Available for natural and IVF pregnancy. Gender determination cannot differentiate Boy+Boy or Boy+Girl.
Available for single and natural pregnancy only, recommended for 12 weeks and over. For twin pregnancy, see NIPT Twin package.
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NIPT, or Non-Invasive Prenatal Testing, is a simple blood test for expecting moms that checks your baby’s DNA to screen for a wide range of genetic conditions.
It’s safe, accurate, and gives you valuable insights into your baby’s health as early as 10 weeks into your pregnancy.
Endorsed by leading medical experts and trusted by healthcare professionals across the globe, MedEx NIPT Test Services are synonymous with quality and reliability.
NIPT is highly accurate, with a detection rate of up to 99% for common chromosomal conditions. Our advanced genetic testing solutions screen for a wide range of disorders, including Down syndrome, Edwards syndrome, and Patau syndrome.
It’s safe and non-invasive, meaning no risk to the mum-to-be or your baby.
It provides important and accurate information about your baby’s health early in your pregnancy
It can detect certain genetic conditions, giving you and your doctor the chance to plan ahead if needed.
It is a simple and easy test that can help you feel more prepared and confident as you move forward in this exciting chapter of your life!
NIPT is a great option for any expecting parents who want early information about their baby’s health. It’s especially recommended for:
Our commitment to safety and accuracy has made us a preferred choice for non- invasive prenatal screening. With a quick turnaround time (7 to 10 days) and affordable testing options, we strive to make our advanced genetic testing accessible to all, providing peace of mind to expecting parents everywhere.
The detailed reports we generate offer clarity and actionable information, ensuring that expecting parents and healthcare providers have all the necessary data at their fingertips.
You will receive the report via email, so you can access it wherever you are. From there, you can get a follow up consultation, if required, with our medical practitioners or any medical practitioner of your choice.
NIPT primarily screens for common chromosomal abnormalities such as trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), and trisomy 13 (Patau syndrome).
Our NIPT Pro package also screens for Mosaic Trisomy 8 and (, Trisomy 16 and X & Y chromosomes abnormalities.
Please note that ta NIPT test may not detect all genetic abnormalities or structural birth defects. It is a screening test, not a definitive diagnostic. Abnormal results should be followed up with confirmatory testing.
While a doctor's referral is not always required for NIPT, it's recommended to consult with a healthcare provider to discuss your options and determine if NIPT is appropriate for your specific situation.
Yes, NIPT can also determine the gender of the baby with high accuracy. This information is included in the test results and can be shared with the parents if desired.
As previously mentioned, noninvasive prenatal testing (NIPT), sometimes called noninvasive prenatal screening (NIPS), is a method of determining the risk that the foetus will be born with certain genetic abnormalities. This testing analyses small fragments of DNA that are circulating in a pregnant woman’s blood. Unlike most DNA, which is found inside a cell’s nucleus, these fragments are free-floating and not within cells, and so are called cell-free DNA (cfDNA).
The analysis utilises Next-Generation Sequencing (NGS) technology to perform high-throughput sequencing of these cfDNA fragments. Advanced bioinformatics algorithms analyse the relative quantities of chromosomal sequences to detect potential aneuploidies, where abnormal ratios may indicate chromosomal conditions. For fetal sex determination, the presence or absence of Y chromosome sequences is evaluated. 10 weeks into your pregnancy.
This test has been validated for singleton pregnancies at or beyond 10 weeks of gestation, when fetal DNA fraction is typically adequate for accurate analysis. Multiple gestations (twins/triplets) may complicate analysis due to mixed fetal DNA sources.
There must be enough fetal cfDNA in the mother’s bloodstream to be able to identify fetal chromosome abnormalities. The proportion of cfDNA in maternal blood that comes from the placenta is known as the fetal fraction. Generally, the fetal fraction must be above 4 percent, which typically occurs around the tenth week of pregnancy. Low fetal fractions can lead to an inability to perform the test or a false negative result. Reasons for low fetal fractions include testing too early in the pregnancy, sampling errors, maternal obesity, and fetal abnormality.
The test is optimized for detecting common trisomies (chromosomes 21, 18, and 13) and sex chromosome aneuploidies in low-risk populations.
Aneuploidy is a condition where a cell or organism has too many or too few chromosomes. It can occur in some or all of the body's cells. Trisomy and Monosomy are a form of aneuploidy.
Most common trisomies
Down Syndrome (Trisomy 21) - 99% test accuracy
Down syndrome is a genetic disorder caused by an extra full or partial cell division of a human's chromosome 21, resulting in intellectual disability, delayed development, a unique body and face, and abnormalities in various body systems. Down syndrome varies in severity among individuals.
Edward Syndrome (Trisomy 18) - 97.4%
Edward Syndrome is a genetic disorder caused by an extra full or partial cell division of a human's chromosome 18 that begins to affect babies when they’re in the womb, and continues to impact their health throughout their life. It’s a rare but serious condition that can cause varied birth defects.
Patau Syndrome (Trisomy 13) - 87.5%
Patau Syndrome is a genetic disorder caused by an extra full or partial cell division of a human's chromosome 13. It is associated with severe intellectual disability and physical abnormalities in many parts of the body most often life threatening.
Rare trisomies
Mosaic Trisomy 8 and 9
A mosaic condition is where an extra copy of chromosome 8, or 9, is present in some cells while other cells remain normal. They can lead to a range of developmental issues and organs defect. Mosaic 9 is typically nonviable.
Trisomy 16
Trisomy 16 is most often detected in miscarriages and rarely results in a live birth.
Sex chromosome abnormalities
Turner Syndrome (XO)
Turner syndrome, a condition that affects only females, results when one of the X chromosomes (sex chromosomes) is missing or partially missing. Turner syndrome can cause a variety of medical and developmental problems, including short height, failure of the ovaries to develop and heart defects.
Triple X Syndrome (XXX)
Females normally have two X chromosomes in all cells — one X chromosome from each parent. In triple X syndrome, a female has three X chromosomes. Many girls and women with triple X syndrome don't experience symptoms or have only mild symptoms. In others, symptoms may be more apparent — possibly including developmental delays and learning disabilities. Seizures and kidney problems occur in a small number of girls and women with triple X syndrome.
Klinefelter syndrome (XXY)
Klinefelter syndrome is a common condition that results when a person assigned male at birth has an extra copy of the X sex chromosome instead of the typical XY. This syndrome may affect testicular growth which can lead to making less of the hormone testosterone. The syndrome also may cause smaller muscle mass, less body and facial hair, and extra breast tissue. The effects of Klinefelter syndrome vary, and not everyone has the same symptoms.
Jacobs syndrome (XYY)
Jacobs syndrome is a rare chromosomal disorder that affects males. It is caused by the presence of an extra Y chromosome. Males normally have one X and one Y chromosome. However, individuals with this syndrome have one X and two Y chromosomes. Affected individuals are usually very tall. Additional symptoms may include learning disabilities and behavioural problems such as impulsivity.
Feel free to contact us with any inquiries regarding MedEx NIPT's prenatal testing, from the accuracy of our results to the process of sample collection and everything in between. Our dedicated team is here to provide you with the information and support you need.
mail@medex.co.th
Enjoy stress-free doctor consultations at MedEx Neo Clinic with prices starting from just 750 THB. You can also access a pool of over 3,000 top specialists at JCI (US)-accredited Thai hospitals in the MedEx Network via our tele-consultation services.
Our advanced prenatal genetic testing solutions screen for a wide range of disorders, including Down syndrome, Edwards syndrome, and Patau syndrome. Advanced MedEx NIPT Testing leverages cutting-edge technology to provide comprehensive insights, enabling early detection and informed decision-making. The detailed reports we generate offer clarity and actionable information, ensuring that parents and healthcare providers have all the necessary data at their fingertips.
Endorsed by leading medical experts and trusted by healthcare professionals across the globe, MedEx NIPT Test Services is synonymous with quality and reliability. Our commitment to safety and accuracy has made us a preferred choice for prenatal screening. With a quick turnaround time and affordable testing options, we strive to make our advanced genetic testing accessible to all, providing peace of mind to expecting parents everywhere.
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Last updated: June 30th, 2022
If you’re dissatisfied with a purchase, We invite You to read our refund and return policy. The following conditions apply to any items or services that you bought from Us.
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For the purposes of this Refund and Return Policy:
You are entitled to cancel Your Order for Packages as per the following terms:
3.1 If you cancel an Order before 4 PM (GMT+7) the next day after making the payment, you can receive an 80% refund. For example, if you want to cancel your reservation, for example, after making it on March 25th, 2022 at 10 AM; You may do so and receive an 80% refund if you notify the company before 4:00 PM on March 26th, 2022.
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