Q. Is there any risk associated with this test?
There is no risk associated with the test. However, since this test involves a needle prick to withdraw the blood sample, in very rare cases, a patient may experience increased bleeding, hematoma formation (blood collection under the skin), bruising or infection at the site of needle prick.
Q. Is a Dual Marker Test especially advised for pregnant ladies above the age of 35 years?
No, this test is also advised for younger women. It helps in screening any birth abnormalities in the fetus before birth. However, after the age of 35 years, the risk of Down syndrome increases, especially in women who have a family history of any birth defects, have given birth to a child with any birth defects previously, or have a history of insulin-dependent type 1 diabetes.
Q. What is the importance of ultrasound in a Dual Marker Test?
An ultrasound is usually advised before a Dual Marker Test. Based on the results of the ultrasound, your doctor will advise a Double Marker Test- First Trimester.
Q. What are the advantages of a Dual Marker Test?
When a Dual Marker Test is done earlier in pregnancy, it helps you to go for other diagnostic tests if the results come back positive. This will allow you and the doctor to make early decisions if needed.
Q. What is Down syndrome?
It is a genetic disorder in which extra genetic material from chromosome 21 gets transferred to the fetus. This transfer affects the development of the fetus leading to abnormal development both physically and mentally. The affected baby will have a small head and short neck, obliquely positioned eyes looking in an upward direction, large tongue coming out of the mouth, flat face, wide hands with short fingers, and lack of muscle tone.
Q. What is Edwards' syndrome?
It is also known as Trisomy 18 which is caused by the development of an extra chromosome 18. Because of this, the normal pattern of development in the baby gets disturbed even before its birth. The effects caused by Trisomy 18 are very complicated compared to Down syndrome. The effects are so severe that it can cause stillbirth (death at the time of birth) of the child.
Q. What is beta hCG?
Beta hCG refers to Beta human Chorionic Gonadotropin. It is a hormone that is produced by the cells in the developing placenta during pregnancy, and its levels increase in the early phase of pregnancy. The role of this hormone is to maintain the function of the corpus luteum (the hormone-secreting structure that develops in an ovary).
Q. What is a Double Marker Test- First Trimester, and why is it performed?
A Double Marker Test- First Trimester is a prenatal screening test that assesses the risk of chromosomal abnormalities in the developing fetus. It is performed to detect potential genetic conditions such as Down syndrome and Edwards’ syndrome.
Q. How early can a Dual Market Test be conducted during pregnancy?
A Dual Marker Test is typically conducted during the first trimester of pregnancy, i.e., between weeks 9 and 13.
Q. What chromosomal abnormalities are screened by a Double Marker Test- First Trimester?
A Double Marker Test- First Trimester primarily screens for Down syndrome (Trisomy 21) and Edwards’ syndrome (Trisomy 18).
Q. Can a Double Marker Test- First Trimester identify the specific chromosomal abnormalities in the fetus?
A Double Marker Test- First Trimester is a screening test and not a diagnostic test, meaning it screens for the risk of chromosomal abnormalities and doesn’t identify the specific abnormality. Confirmatory tests are required for a definitive diagnosis.
Q. What if a Dual Marker Test is missed?
Suppose you miss the recommended Dual Marker Test time frame; in that case, your doctor may recommend alternative tests, such as a quad marker screening test (typically performed between the 15th and 21st week of pregnancy), depending on the stage of pregnancy.
Q. What is the difference between a Double Marker Test- First Trimester and an NT scan?
A Double Marker Test- First Trimester is a blood test, whereas an NT scan is an ultrasound. The doctor recommends both these tests during the first trimester to screen for the possible risk of chromosomal abnormalities in the unborn child.
Q. Should a Double Marker Test- First Trimester be done on an empty stomach?
This test is a non-fasting blood test. Unless the doctor instructs otherwise, you can eat or drink normally before the test.
Q. Can I book a Double Marker Test- First Trimester in Navi Mumbai?
Yes, you can book a Double Marker Test- First Trimester in Navi Mumbai with Tata 1mg Labs. The test can be booked easily, is affordable, and comes with an easy-to-understand report.
Q. Is home sample collection possible for a Double Marker Test- First Trimester in Navi Mumbai?
Yes, home sample collection is possible for a Double Marker Test- First Trimester in Navi Mumbai with Tata 1mg Labs. You can also choose a date and time that suits your schedule for sample collection.
Q. How can I book a Dual Marker Test with Tata 1mg Labs in Navi Mumbai?
The booking process for a Dual Marker Test with Tata 1mg Labs in Navi Mumbai is straightforward and hassle-free. Follow these steps to schedule a test online: 1). Go to the Lab Tests section on the Tata 1mg website. 2). Add your preferred test to the shopping cart. 3). Choose a time and day that works for you as long as you also take the essential prerequisites into account. 4). A confirmation notification will be sent to you with all the details once the booking is complete.
Q. What is the cost of a Double Marker Test- First Trimester in Navi Mumbai?
Tata 1mg Labs allows you to book tests at an affordable price in Navi Mumbai. A Double Marker Test- First Trimester can be booked at a pocket-friendly budget of Rs. 1729.
Q. How long does it take Tata 1mg Labs to provide the reports of a Double Marker Test- First Trimester in Navi Mumbai?
We at Tata 1mg Labs recognize the value of prompt results. We strive to deliver test results with quick turnaround times so you can receive the information promptly. The reports of a Dual Marker Test in Navi Mumbai are often provided in 72 hours.