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Double Marker Test Price in Dubai
599 AED 499 AED (Limited Time Offer)
The Double Marker Test is a common prenatal screening test used to identify the risk of certain chromosomal abnormalities in a developing fetus, specifically Down syndrome (trisomy 21) and Trisomy 18. It is mostly performed during the first trimester, usually between the 9th and 13th weeks of pregnancy.
If you’re expecting and want to learn more about your baby’s health, don’t wait and book our Double Marker Test to assess the risk of chromosomal abnormalities, such as Down syndrome and Trisomy 18. This screening test provides valuable insights into your pregnancy, helping you understand the likelihood of these conditions.
You can easily find the Double Marker Test Price or Double Marker Test Cost by searching for Double Marker Test Near Me, making it convenient to access this essential prenatal screening service. At Royal Health Group, we offer the Double Marker Test now available at a limited-time offer for only AED 499!
Don’t leave your baby’s health to chance. Schedule your Double Marker Test today and take the first step toward a safer and informed pregnancy journey!
The results of the Double Marker Test are typically presented as a risk ratio, which is a comparison of the probability of a fetus having the condition versus not having it. For example, a risk ratio of 1:100 means there’s a 1 in 100 chance the baby could have the condition.
The Double Marker Test is very important to assess the risk of the baby being born with genetic conditions, particularly Down syndrome (trisomy 21) and Trisomy 18. It is not a diagnostic test, meaning it cannot definitively confirm or rule out these conditions but helps to identify pregnancies at higher risk for further testing or monitoring.
The Double Marker Test is a blood test taken from the pregnant woman, which measures the levels of two substances in her blood:
These markers, when combined with other factors such as maternal age, weight, and medical history, help estimate the likelihood of the baby having certain conditions. Additionally, Non Invasive Prenatal Testing (NIPT) can provide a more comprehensive assessment of the risk for chromosomal abnormalities with a high degree of accuracy.”
If the Double Marker Test shows an increased risk for Down syndrome or Trisomy 18, the next step usually involves more invasive diagnostic tests, such as:
These tests can provide a more definitive diagnosis, though they do come with a small risk of miscarriage.
If you’re looking for a Double Marker test or searching for the Double Marker Blood Test Price, look no further. Royal health group in Dubai now offers the convenience of at home Double Marker testing. You can easily book your lab test from the comfort of your home by calling +971 50 844 3803 today.
A low risk indicates that the likelihood of chromosomal abnormalities, such as Down syndrome or Trisomy 18, is minimal.
A moderate risk suggests that the chances of abnormalities are slightly higher than usual. In these cases, we recommend further testing, such as the Triple Marker Test or chorionic villus sampling (CVS), to gain a more detailed understanding of the fetus's health and reduce uncertainty.
A high risk indicates a significantly higher likelihood of chromosomal abnormalities. When this occurs, doctors typically recommend more invasive diagnostic procedures, like amniocentesis, to confirm whether the fetus has a genetic condition and to explore the next steps for care and planning.
You should take the Double Marker Test to assess the risk of chromosomal abnormalities like Down syndrome and Trisomy 18 early in pregnancy.
Other tests, such as the Triple Marker Test and Non Invasive Prenatal Testing (NIPT), can provide additional screening and risk assessment for chromosomal abnormalities.
Yes, the Double Marker Test can be recommended for women with a family history of genetic disorders or those who are at a higher risk due to factors like age or medical history.
The Double Marker Test costs AED 499Â
The Double Marker Test is generally offered to all pregnant women, but it’s especially useful for those who are at a higher risk of chromosomal abnormalities. This includes women over 35, those with a family history of genetic conditions, or women who have had previous pregnancies with chromosomal abnormalities.
The Double Marker Test is typically performed between the 9th and 13th weeks of pregnancy. This timing helps to accurately measure the levels of PAPP-A and hCG in the mother’s blood.
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For getting Double Marker Test at home . Call Royal Health Group Home Care on +971 50 844 3803Â
Yes, the test is non invasive and involves only a blood taken from the mother, making it safe for both the mother and the baby.
Absolutely. The test involves a simple blood test taken from the mother. The blood sample is then analyzed to measure the levels of PAPP-A and hCG.
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The Double Marker Test focuses on two specific markers (PAPP-A and hCG) and provides a risk assessment for Down syndrome and Trisomy 18.
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