Why is this Prenatal Screening test your best option?
There is a variety of prenatal screening options to choose from. However, unlike the non-invasive prenatal screening test, traditional screening methods provide a lower accuracy rate and higher false positive rates (as shown in the image below). A false positive is where you receive a positive result for a test, when you should have received a negative result.
In addition, invasive diagnostic tests such as Amniocentesis and Chorionic villus sampling (CVS) involve risks such as a 0.5 to 1% chance of miscarriage, leakage of the amniotic fluid or damage to the baby’s limbs. On the contrary, this non-invasive test is considered 100% safe since it only requires a 10ml maternal blood sample and does not pose any risks to the mother or the unborn baby. One should also note that this is the most validated prenatal screening test on the market with a published study based on the outcomes of circa 147,000 pregnancies and over 1 million tests performed worldwide to date. But it doesn’t stop there, this test also allows you to discover the sex of your baby at no extra charge! Should you be interested in this service, please make sure to select the respective option when ordering the test.
This test can detect the following Chromosomal Abnormalities:
A trisomy is a type of aneuploidy (an abnormal number of chromosomes) in which there are three chromosomes instead of the normal two.
|Trisomy 9||Patau Syndrome (Trisomy 13)||Trisomy 16|
|Edward’s syndrome (Trisomy 18)||Down Syndrome (Trisomy 21)||Trisomy 22|
The below lists of abnormalities and disorders are also tested for no additional cost!
SEX CHROMOSOME ABNORMALITIES
A sex chromosome aneuploidy is a numeric abnormality of an X or Y chromosome, with the addition or loss of an entire X or Y chromosome.
|Turner’s syndrome (XO)||Triple X (XXX)|
|Klinefelter’s syndrome (XXY)||Jacob Syndrome (XYY)|
DELETION & MICRODELETION SYNDROMES
Deletion syndromes are a group of clinically recognisable disorders caused by the deletion of a small chromosomal segment.
|16p12.2-p11.2 deletion||1p36 deletion||2q33.1 deletion|
|Angelman Syndrome||Cri-du-chat Syndrome||DiGeorge Syndrome 2|
|Jacobsen Syndrome (11q23)||Prader-Willi Syndrome||Van der Woude Syndrome|
How does the test work? What is the Turnaround time?
The non-invasive screening test only requires a small blood sample of 10ml from the expectant mother (please note that a qualified person is required to collect the sample via a standard medical blood draw). Once your sample is received at the laboratory, scientists use whole genome sequencing technology and four different proprietary bioinformatics analysis pipelines to analyse the foetal DNA and accurately confirm or exclude the presence of a genetic abnormality. For instance, scientists can determine that the expectant mother is carrying a baby with Down’s syndrome since the ratio of genetic material associated with chromosome 21 will be higher due to the extra, third copy of that chromosome. Results for this test are available in as little as 10 to 14 working days! Please note that turnaround time starts from the moment samples reach the laboratory.
For complete peace of mind order this highly advanced screening test today, starting from only €395!
Even though this test is considered as the most accurate screening test available for Trisomy 21, other Trisomies and specific chromosomal disorders, it is important to note that it still remains a screening test and not a diagnostic test, and that it does not screen for all chromosomal conditions. Please also note that this test cannot replace diagnostic tests such as Amniocentesis and Chorionic villus sampling but it can help expectant mothers avoid the need to undergo these invasive tests.