NIPT TEST
Non-invasive Prenatal Testing - NIPT TEST
NIPT TEST from AED-1499/-
Non-invasive Prenatal Testing - NIPT TEST
- Simple & Safe blood test
- >99% accuracy
- Faster result from 10 to 15 days.
- Efficient - multi syndrome detection
Comparison Of NIPT test
| Test Name | Panorama AI NIPT Popular NIPT Test | NIPS (NIPT) by NGS | NIPT-23 |
| Weeks | >9 weeks 0 days | >10 weeks 0 days | >10 weeks 0 days |
| Reports | 10 to 12 days | 12 to 15 days | 10 to 12 days |
| Down Syndrome (trisomy 21) |  | | |
| Edward Syndrome (trisomy 18) | | | |
| Patau Syndrome (trisomy 13) | | | |
| Triploidy | |  | |
| Sex Chromosome Aneuploidy X0, XXX, XXY, XYY | | | |
| Fetus Gender | (Zero Error) | | |
| Identify Twin Baby Gender Seperately | (Boy,Boy; Boy,Girl; Girl,Girl) | | |
| DiGeorge syndrome (22q11.2 deletion) | (@ Additional charges) | (@ Additional charges) | (@ Additional charges) |
| Additional 4 Microdeletions | (@ Additional charges) | (@ Additional charges) | (@ Additional charges) |
| SNP technology | | | |
| AI technology | | | |
| Identify Mom & Baby DNA separately | | | |
| Free Genetic Counselling Session | | | |
| Price in AED | 2,200/- | 1,499/- | 2,900/- |
Panorama Next-Gen NIPT Test. As early as 9 weeks.
Panorama is the most advanced NIPT test which uses the SNP based technology to delivers results with more insights and greater accuracy. This is the most rigorously validated NIPT Test Get free Genetic information sessions before and after the test to clarify all your doubts regarding the test and result.
Panorama Next-Gen NIPT Test
| Test Parameters | panorama NIPT Standard AED-2500 AED 2200 | panorama NIPT Standard + 22q11.2 deletion AED-3000 AED 2500 | panorama NIPT Standard + all 5 microdeletions AED-3800 AED 3500 |
| Down Syndrome (trisomy 21) | | | |
| Edward Syndrome (trisomy 18) | | | |
| Patau Syndrome (trisomy 13) | | | |
| Triploidy | | | |
| Turner syndrome (monosomy X) | | | |
| XXX syndrome (47,XXX) | | | |
| Klinefelter syndrome (47,XXY) | | | |
| Jacobs syndrome (47,XYY) | | | |
| Fetus Gender | | | |
| 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) | | | |
NIPT 23
| Test Parameters | NIPT23 SAGE Standard AED- 2900 | NIPT23 SAGE Plus AED-3800 |
| Down Syndrome (trisomy 21) | | |
| Edward Syndrome (trysomy 18) | | |
| Patau Syndrome (trisomy 13) | | |
| sex chromozome aneuploidy Turner syndrome (mX), Klinefelter syndrome (XXY), XYY & XXX Syndrome | | |
| Fetus sex | | |
| Other Chromosome Aneuploidies | | |
| 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. | | |
Limited Scope
It’s important to note that the NIPT test has limitations in terms of its scope. It primarily serves as a screening test for common chromosomal abnormalities and does not provide information about other genetic disorders or birth defects. False-positive and false-negative results are also possible, and positive results require confirmation with invasive diagnostic testing.
Conditions Screened For
Panorama screens for common genetic conditions that are caused by extra or missing chromosomes in the baby’s DNA. Because Panorama uses a unique technology to truly distinguish between the mother’s and the baby’s DNA, it is the only NIPT test that screens for triploidy, and it has the highest accuracy in determining the gender of the baby (optional). Some conditions, such as Down syndrome, are caused by extra copies of a specific chromosome. Others, such as microdeletions, occur when a chromosome is missing a small piece of genetic information. Microdeletions affect pregnancies equally, regardless of maternal age.
TRISOMIES
XY CHROMOSOME ABNORMALITIES
MICRODELETIONS*
Microdeletions screened in NIPT test
Microdeletions are chromosomal abnormalities characterized by the loss of a small piece of genetic material from a chromosome. In the context of NIPT, microdeletions refer to the detection of certain specific microdeletion syndromes during prenatal screening. These syndromes involve the absence of a small segment of genetic material, typically ranging from a few kilobases to several megabases.
The comprehensive NIPT that screens for a range of chromosomal abnormalities, including certain microdeletion syndromes. Some of the common microdeletion syndromes that may be screened by NIPT include:
1p36 deletion syndrome
It is a genetic syndrome characterized by birth defects, intellectual disability, and other serious medical issues. 1p36 deletion syndrome is caused by a deletion in the region of 1p36. Key features of this syndrome include: characteristic craniofacial features, intellectual disability, seizures, skeletal abnormalities, and brain and heart defects. Lifespan is variable, but can be normal.
4p- syndrome
This is a rare genetic syndrome characterized by birth defects, intellectual disability, and other serious medical problems. 4p- syndrome is caused by a deletion in the region of 4p16.3. Key features of the syndrome include: prenatal-onset growth deficiency followed by postnatal growth retardation and hypotonia with muscle underdevelopment, typical craniofacial features in infancy consisting of a characteristic appearance of the nose, microcephaly, intellectual disability of variable degree, seizures, skeletal anomalies, congenital heart defects, hearing loss (mostly conductive), urinary tract malformations, and structural brain abnormalities. Life expectancy varies depending on severity of features.
5p- syndrome
It is a genetic syndrome charac-terized by birth defects, intellectual disability, and other serious medical issues. 5p- syndrome is caused by a deletion in the region of 5p15.2. Key features of this syndrome include: significant intellectual disability, speech delay, cat-like cry, dysmorphic features, microcephaly and 10% mortality in first year.
Prader-Willi syndrome (PWS)
is a rare genetic condition that causes difficulty feeding and failure to thrive in infancy, with obesity, developmental delay, and other medical prob-lems as the child gets older. NIPT is only able to detect PWS caused by a deletion, which accounts for ~70% of cases; the remaining cases are caused by different underlying molecular mechanisms. Angelman syndrome (AS) is a rare genetic syndrome that includes intellectual disability and other serious medical problems. NIPT is only able to detect AS caused be a deletion, which accounts for ~68% of cases; the remaining cases are caused by different underlying molecular mechanisms.
22q11.2 deletion syndrome
is a genetic syndrome that is variable in presentation. Many features have been reported, yet individuals with this syndrome may have different presentations from one another. Key features of this syndrome are variable, but include: intellectual disability, heart defects, palatal abnormalities, immune deficiency, and dysmorphic features. Life span is usually normal, but can vary depending on severity of features.
Why Choose PH Diagnostics?
FAQ's
The NIPT test procedure involves three straightforward steps:
- A blood sample is taken from the expectant mother.
- The blood sample is then sent to a specialized facility for laboratory analysis.
- Typically, the results are available within two weeks.
