Non-Invasive Prenatal Test at Your Doorstep
By Our Experts & DHA Certified Medical Staff
Get NIPT Test at your place in just 3 easy steps!
1. Book An Appointment
2. Nurse At Your Place
Experienced & DHA Certified Nurse will be at your door-step in just 30-45 minutes anywhere in Dubai.
3. Fast & Accurate Results
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Physician Reviewed Results
Same Day Results
From The Most Trusted Lab
Direct Contact with senior medical team
NIPT Test at Home in Dubai
The non-Invasive prenatal test (NIPT) is one of the most sought-after tests for multi syndrome detection with 99% accuracy. This test assesses fetal DNA from samples taken from the mother and tested at the international standard laboratory of Aims Healthcare in Dubai.
For performing a NIPT test at home, our qualified doctors and nurses set a pattern of around 10 weeks gestation throughout the pregnancy. We elevate the process by bringing our services to your home so the mother can enjoy the comfort of her house and don’t have to travel all the way to the hospital or clinic. Our methods are result-proven and accurate that adhere to the standards set by the Dubai Health Authority.
Secure & Standardized NIPT Test at Home
Our NIPT Test at Home using Next-Generation Sequencing (NGS) technology is a comprehensive test that detects the presence of any chromosome that might lead to birth with the syndrome. It helps us understand the pregnancy of the mother and formulate a healthy routine for a well birth of a child.
| Test Parameters | Standard | Premium |
| Down Syndrome (trisomy 21) |  |
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Edward Syndrome (trisomy 18) | |
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Patau Syndrome (trisomy 13) | |
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Turner syndrome (monosomy X) | |
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XXX syndrome (47,XXX) | |
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Klinefelter syndrome (47,XXY) | |
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Jacobs syndrome (47,XYY) | |
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Fetus Gender | |
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1p36 deletion syndrome (1p36 deletion) | - | |
Wolf-Hirschhorn syndrome/4p- syndrome (4p16.3 deletion) | - | |
Cri-du-Chat syndrome/5p- syndrome (5p15.2 deletion ) | - | |
Prader-Willi and Angelman syndromes (15q11.2-q13 deletion) | - | |
DiGeorge syndrome (22q11.2 deletion) | - | |
Panorama Next-Gen NIPT Test at Home
We provide the most advanced NIPT test at home that is as early as 9 weeks, using the SNP-based technology to deliver accurate results and deep insights regarding the normality of pregnancy. This test is validated and provides the perfect information regarding the pregnancy process.
| Test Parameters | Panorama NIPT Standard | Panorama NIPT Standard + 22q11.2 deletion | Panorama NIPT Standard + all 5 microdeletions |
| Down Syndrome (trisomy 21) | |
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| Edward Syndrome (trisomy 18) | |
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| Patau Syndrome (trisomy 13) | |
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| Triploidy | |
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| Turner syndrome (monosomy X) | |
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| XXX syndrome (47,XXX) | |
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| Klinefelter syndrome (47,XXY) | |
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| Jacobs syndrome (47,XYY) | |
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| Fetus Gender | |
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| DiGeorge syndrome (22q11.2 deletion) | - | |
|
| 1p36 deletion syndrome (1p36 deletion) | - | - | |
| Wolf-Hirschhorn syndrome/4p- syndrome (4p16.3 deletion) | - | - | |
| Cri-du-Chat syndrome/5p- syndrome (5p15.2 deletion ) | - | - | |
| Prader-Willi and Angelman syndromes (15q11.2-q13 deletion) | - | - | |
Harmony NIPT Test at Home
Harmony is another NIPT blood test that screens for the detection of specific chromosomes during a pregnancy situation as early as 10 weeks. At this point, your blood contains a tiny baby’s DNA, and this Harmony NIPT test gives perfect information about your child’s birth.
| Test Parameters | NIPT Harmony Standard | NIPT Harmony Premium |
| Down Syndrome (trisomy 21) | |
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Edward Syndrome (trisomy 18) | |
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Patau Syndrome (trisomy 13) | |
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Assessment of risk of X and Y chromosome aneuploidies, including monosomy X, XXX, XXY, XYY and XXYY. | |
|
Fetus sex | |
|
Microdeletions | - | |
NIPT23 NIPT Test at Home
Our NIPT23 Test at home caters to autosomal aneuploidies, sex chromosome aneuploidies, and microdeletions. The test parameters with two categories are mentioned in the table.
| Test Parameters | NIPT23 SAGE Standard | NIPT23 SAGE Plus |
| Down Syndrome (trisomy 21) | |
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Edward Syndrome (trysomy 18) | |
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Patau Syndrome (trisomy 13) | |
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sex chromozome aneuploidy Turner syndrome (mX), Klinefelter syndrome (XXY), XYY & XXX Syndrome | |
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Fetus sex | |
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| Other Chromosome Aneuploidies | |
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| Microdeletions DiGeorge Syndrome, 1p36 Deficiency Syndrome, Pride Wiley Syndrome (Square Willy Syndrome), Ang Joman's Syndrome (Angel Syndrome), Cat Cry Syndrome, and Wolf-Hew Hung's Syndrome. | - | |
Chromosomes and Syndromes Detection through NIPT Test at Home
The non-invasive prenatal test by Aims Healthcare is specifically devised by keeping all the international standards and protocols set by Dubai Health Authority. Our test centers on testing the mother’s blood for the abnormalities of the unborn. Here are a few chromosomes and disorder detection our world-class medical team of doctors and nurses do right at your home to provide uncompromised comfort and satisfaction.
| DISORDER | CHROMOSOME | DESCRIPTION | PREVALENCE |
| Down Syndrome | Trisomy 21 | Not all, but some of the pregnancies with trisomy 21 end up in pregnancy loss. But it also leads to living birth with physical and intellectual disability. This chromosome leads to heart defects, low muscle tone, and indifferent facial features. Furthermore, a child can also develop cognitive impairment that ranges from mild to severe. Not only this, but the child may also develop helpless medical conditions such as Alzheimer’s disease, leukemia, thyroid problems, and hearing impairment. Upon the birth of a child, they require special treatment in order to go about their regular lives. | The occurrence of Trisomy 21 happens in 1 in 800 live births. |
| Edwards Syndrome | Trisomy 18 | This chromosome leads to miscarriage or stillbirth. However, the live birth of a child results in specific disabilities and abnormalities of particular organs. For example, the significant results of Edwards syndrome are improper brain functioning, heart defects, musculoskeletal problems, cleft lip and palate, and even low birth weight. Another devastating fact is that nearly 10% of all babies born with Edwards syndrome only live for about a year or so. | Trisomy 18 is a syndrome that results in 1 in 6000 births. |
| Patau Syndrome | Trisomy 13 | This chromosome also results in miscarriage or a stillbirth. However, the babies born with this syndrome have severe intellectual disabilities and abnormalities. Improper heart and brain functioning, cleft lip and palate, and holoprosencephaly are some of the significant abnormalities a child has to suffer. |
The rate of occurrence of trisomy 13 is relatively low. |
| Turner Syndrome | Monosomy X | It is a rare condition that is caused by one X sex chromosome and the absence of a second yet same chromosome instead of two sex chromosomes. This missing chromosome can be either father or mother. Moreover, pregnancies with the Monosomy X chromosome result in learning disabilities and other variables. This also includes heart malfunctioning, short stature, kidney abnormality, etc. |
This syndrome usually occurs in 1 in 2500 females. |
| XXX Syndrome | 47, XXX | XXX syndrome is another pregnancy impairment that results in a child's genetic disorder. In this case, the mother develops three X chromosomes instead of two X chromosomes from the father and mother. In order to cure this, the NIPT test at home by Aims Healthcare is highly effective in which the NIPT is done on the fluid surrounding the fetus, tissue from the placenta, or the blood from the mother. |
This syndrome usually occurs in 1 in 1000 females. |
| Klinefelter Syndrome | 47, XXY | Klinefelter syndrome is associated with the male X sex chromosome. Here the male has two copies of X and Y chromosomes, resulting in a type of syndrome. This usually happens with having variable phenotypes. Pregnancies with this syndrome result in learning disabilities, delayed speech, taller stature, language development, etc. Moreover, it also results in infertility which is not the case with all the cases, yet happens with a few. | The birth rate with XXY syndrome is 1 in 600 males. |
| Jacobs Syndrome | 47, XYY | Jacobs syndrome is also linked to male sex chromosomes where the pregnancy results in one X chromosome and two Y chromosomes, unlike the usual copies of one X and Y chromosomes. The child born with this syndrome may face language development speech abnormalities with an unusual taller stature. |
The birth rate of XYY syndrome is 1 in 1000 males. |
| 1p36 deletion syndrome | 1p36 deletion | This genetic syndrome results in congenital disabilities, intellectual disabilities, and medical issues in the long term. It further results in heart defects, brain abnormalities, and craniofacial features. The lifespan is variable in it but can be normal with treatments. | The female ratio is 2:1 with this syndrome. Usually, happen to 1 in 4000 cases. |
| Wolf-Hirschhorn syndrome | 4p16.3 deletion | It is a rare genetic syndrome that also results in various medical issues. The primary issues in this syndrome are growth deficiency that is followed by postnatal growth retardation and hypertonia with muscle underdevelopment. Moreover, seizures, skeletal anomalies, and urinary tract malformations are some, to name a few. | The cases are for 1 in 50,000 newborns have this condition, with females more prone to catching this. |
| Cri-du-Chat syndrome | 5p15.2 deletion | It is another genetic syndrome that is characterized by birth defects, medical issues, and other disabilities. It also includes speech delay, dysmorphic features, and microcephaly disability that has 10% mortality in the first year. |
Every 1 in 20,000 births is with this syndrome. |
| Prader-Willi and Angelman syndromes | 15q11.2-q13 deletion | Another rare genetic condition results in difficulty in feeding and failure to thrive in infancy, with obesity and growth delay. Moreover, intellectual disability and some other medical concerns also become inevitable with this syndrome. |
Births with PWS and AS occur in 1 in 20,000 - 25,000. |
| DiGeorge syndrome | 22q11.2 deletion | It is a genetic syndrome that is variable in presentation. Births with this syndrome include disability in intellectual, heart defects, and other palatal abnormalities with immune deficiency and dysmorphic features. | This condition can victimize 1 in 4000 births. |
How Does Aims Healthcare Help You?
The NIPT test at home in Dubai by Aims Healthcare is performed holistically with top-notch technology and international qualified and DHA-approved medical teams. Our unparalleled expertise in a NIPT test at home, hotel, or anywhere you prefer offers the following benefits;
- The non-invasive prenatal test by Aims Healthcare right at your home provides a perfect report that helps you understand your pregnancy better
- Our teams are responsible for checking the fetal structure and check the birth stage to help you undergo the required blood test so that the problems with chromosomes and syndromes can easily be diagnosed and cured
- We let the mother and father know about the abnormal number of chromosomes present in each cell. Here the particular focus is on the trisomies that become the primary factors of different syndromes
- Our most sought-after medical team undermines the child’s growth and birth and offers tests, medication, and healthcare practices to eliminate the chances of miscarriage or stillbirth
- Our NIPT test at home also helps in gender detection so that parents can plan the birth of a child accordingly. This happens with a clinically-proven accurate test around 7 weeks into pregnancy
Frequently Asked Questions
At Aims Healthcare, we provide clinically-proven methods and services to our patients. Our prior focus is on the betterment of mother and child. As for the starting period of the NIPT test at home, our medical experts generally recommend beginning any time after 10 weeks in pregnancy and is usually before 21 weeks.
The doctors at Aims Healthcare strictly ask mothers not to fast before the NIPT test at home or any other location as it doesn’t a requirement. You can drink or usually eat before the blood test and the ultrasound.
NIPT blood test at home reveals the gender of the baby. Our NIPT test service at home profoundly examines the chromosomes and tells the gender of your baby. However, this information will only be revealed if the mother and father agree to ask about it.
Aims Healthcare is a leading name for providing premium healthcare services to patients throughout Dubai. We focus on providing accurate testing service at home to exceed clients’ expectations and build solid relationships with them. So, our NIPT test facility at home for syndrome detection gives accurate results by reaching the accuracy levels of 99%.
Now for the inappropriate fetal DNA, the reasons are many. A lot of people focus on getting the NIPT test earlier than the duration, which shows low fetal fractions. Sometimes the sampling errors, maternal obesity, and fetal abnormality are also insufficient fetal DNA. But the NIPT test at home by our professional doctors and nurses focuses on providing an accurate report, and that too if the timeframe has met the requirements.
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