What is the Double Marker Test?
The test results produce a prenatal screener determining two substances in a woman's blood: Free Beta-hCG and associated with plasma pregnancy protein A. Biochemical markers are available to assess the risk of chromosomal abnormalities in a fetus, for instance, Down syndrome (Trisomy 21) Edwards syndrome (Trisomy 18).
At Dr. Aravind's IVF, Best IVF Centre in Bangalore, we help couples along the significant transitional milestones of parenthood-related journeys with advanced screenings such as the double marker test. This test is important in pregnancy for evaluating the fetus's health and for early detection of possible chromosomal conditions. A speedy diagnosis gives expert care so that the couple can make informed decisions and continue their journey with confidence and peace.
The journey of pregnancy is beautiful. But it is fraught with decisions and timed tests. One of these is the Double marker test, which checks on the baby’s health at a very early stage in the pregnancy. It not only looks at health, but can provide a huge amount of information about chromosomal abnormalities, which can help inform the parents and their doctors.
The Purpose of Double Marker Test is not to make a diagnosis but to definitely screen for pregnancies that may be at a higher risk for having some chromosomal anomalies. It is generally recommended to be performed in the first trimester so an intervention can be made if necessary or testing can be done such as chorionic villous sampling (CVS) or amniocentesis.
Even though they are both engaged in early pregnancy care, the double marker test does not confirm pregnancy. Early pregnancy confirmation can be done by UPT, ultrasound, or blood tests. The double marker test is done after pregnancy is confirmed to assess fetal health through risk analysis from blood biomarkers and maternal age.
It is usually done between the 11th and 14th weeks of pregnancy, and that time is very important because it is during this period that the biochemical markers are best determined. Delayed testing will lessen the effect of the test and might be offered other types of screenings.
Normal range of Double Marker Test are best understood as being complicated. They differ according to maternal age, weight, and gestational age. Results of the standard test are usually placed under the categories screen positive or screen negative. Screen negative means low-risk pregnancies and a screen positive indicates a higher risk and a probable need for further testing.
A positive result could indicate a higher chance of Down syndrome rather than a genetic disorder. It usually indicates to a doctor that it should conduct more testing to confirm or rule out the problem. Regarding your outcome, always get advice from a certified professional.
If you are in search of the Best IVF Center near me, then look to Dr. Aravind's IVF, a name synonymous with trusted reproductive health. They offer comprehensive pre-pregnancy and prenatal screening services, including double marker testing. Personalized treatment plans and advanced technology put Dr. Aravind's IVF on the path of offering the best start to hopeful parents in their fertility journey.
In regards to the Best IVF Clinic with High Success rate, Dr. Aravind's ranks consistently at the top. A team of experienced doctors brings the concept to reality to ensure the very best patient care from the earliest screen, including the double marker test, to successful embryo transfers. With science and the touch of compassion, the clinic achieves out-of-the-world results in both natural and assisted conception.
Whether you're struggling with infertility issues, suffering from complications, or in need of perinatal testing, one of the key considerations you have to make is how to find the right Female Infertility Clinic near me. Dr. Aravind's IVF is a premier fertility treatment and diagnostic testing centre, interested in achieving a safe and timely pregnancy. Their treatment is female-patient focused, and will enable the team to address all necessary hormonal and genetic factors involved in fertility. This allows proper management regarding leading you through all the right testing at the right time.
When you have some of the Top IVF Specialists in India working for your care - you're probably going to have a better outcome. Dr. Aravind's IVF also has some of the best fertility doctors in India working for you. The doctors at Dr. Aravind's IVF continuously keep themselves informed about the latest developments in reproductive science. Whether it's IVF, ICSI, or even do prenatal screening like the double marker test, the trained team at Dr. Aravind's IVF provides unparalleled support in the entire process.
A double marker test is an insight into the early development of your baby, and much more than just a number. While such results do not equate to a diagnosis, they may inform some risks which can be further evaluated for reassurance or prompt attention. Complications should always be checked by your trusted fertility or obstetrics specialist so that you know what your test results actually mean and what your next steps are.
Contact us +91 90 2012 2012 to Book your Appointment and find out about our IVF Cost and take the first step in establishing your future with one of the leading IVF centres of India.
The double marker test is a type of prenatal screening test that indicates the fetus's risk of developing chromosomal abnormalities. This is evaluated in terms of risks of Down syndrome-Trisomy 21, Edwards syndrome -Trisomy 18,The double markers are done exclusively within the first trimester of pregnancy which falls between 11 to 14 weeks.
Usually it is done between the 11th and 14th week of pregnancy and that time is very crucial, as during this window biochemical markers are determined best. Otherwise, late testing will cause a reduced effect of the test and there might be other types of screenings.
The double-marker test provides estimates based on the risk for Down syndrome, Edward syndrome, or other chromosomal abnormalities that are unconfirmed and therefore considered only screening tests and not confirmatory tests. It is not really essential for the test during pregnancy, but it is highly recommended for women above 35 years of age or those with a family history of genetic disorders.
Individually, these two tests are applied as prenatal screening tests against the risk of chromosomal abnormality in the developing fetus. Different approaches are taken and different parameters are measured in each of these tests. Via ultrasound, the NT scan measures the transducer placement at the nuchal area and the amniotic fluid collection behind the neck of the fetus; the double marker is a blood test that looks at serum biochemical markers of pregnancy in the mother's blood.
The risk of pregnancy with Trisomy 21 or Down syndrome increases with age, and especially from 35 years onwards. While older mothers run a higher risk, it is younger women who have more babies with Down syndrome because the number of deliveries in this category tends to be higher.
