Triple Marker Test

₹4440 ₹3552

Report Time

After 3 Days

No Fasting Required

FREE

Home Sample Collection

Age Group

Parameters Included

Recomended for

Female

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Health Advisor

Triple Marker Test

No Fasting Required

Report Time

After 3 Days

Parameters Included

₹4440 ₹3552

Get a CALLBACK from our
Health Advisor

Understanding the Test

Test Measures

City Price Info

FAQs

Understanding the Triple Marker Test

The Triple Marker Test, or Triple Screen Test, is a second-trimester non-invasive blood test usually performed between weeks 15 and 20 of pregnancy. This test screens for the risk of some chromosomal defects and neural tube defects in the unborn child.

Triple Marker Test Measures

The key components measured in this test include Alpha-fetoprotein (AFP), Human Chorionic Gonadotropin (hCG), and Estriol (uE3). AFP is a protein produced by the fetal liver, and abnormal levels may indicate neural tube defects or chromosomal disorders. hCG is a hormone produced by the placenta, and elevated levels can suggest an increased risk of Down syndrome. Estriol, an estrogen secreted by both the fetus and placenta, tends to be low in certain chromosomal disorders. By analyzing the levels of these substances, medical professionals can estimate the risk of specific fetal abnormalities, allowing for early diagnosis and timely intervention.

Triple Marker Test Price For Other Cities

Location	Price
Triple Marker Test Price in Dehradun	4590
Triple Marker Test Price in Mohali	4590
Triple Marker Test Price in Chandigarh	4590
Triple Marker Test Price in Panchkula	4590
Triple Marker Test Price in Zirakpur	4590
Triple Marker Test Price in Gurgaon	4440
Triple Marker Test Price in Delhi	4440
Triple Marker Test Price in Noida	4440
Triple Marker Test Price in Greater Noida	4440
Triple Marker Test Price in Faridabad	4440
Triple Marker Test Price in Ghaziabad	4440
Triple Marker Test Price in Mumbai	3050
Triple Marker Test Price in Nagpur	3080
Triple Marker Test Price in Lucknow	4200

Purpose and Significance of Triple Marker Test

Triple Marker Test is mainly done to evaluate the risk of:

Down Syndrome (Trisomy 21): A chromosomal abnormality caused by an extra chromosome 21.
Edwards Syndrome (Trisomy 18): A condition that occurs due to an extra chromosome 18, resulting in severe developmental delay.
Neural Tube Defects: Similar to spina bifida, where the spinal cord doesn't form properly.

It is crucial to realize that this is a screening test and not a diagnostic test. An abnormal test doesn't confirm the presence of a condition but rather indicates that further diagnostic testing is needed.

Who Should Undergo the Triple Marker Test?

Although the Triple Marker Test is not required, it's normally recommended for:

Women aged 35 years and older.
Those with a family history of genetic disorder.
Those who've already had an earlier child born with a defect.
Conceptions obtained by assisted reproductive technologies.
Women with certain medical conditions, e.g., diabetes.

Talking to a doctor can help determine whether this test is appropriate for your specific situation.

Procedure: What to Expect

The Triple Marker Test is a simple blood test:

Preparation: No preparation is needed.
Blood Collection: A healthcare professional will draw a small blood sample from your arm.
Laboratory Analysis: The sample is analyzed to measure the levels of AFP, hCG, and uE3.
Result Interpretation: The results are interpreted together with others like maternal weight, age, ethnicity, and gestational age to ascertain levels of risk.

Results often take a week to become ready.

Interpretation of Results

Results are presented in form of risk assessment:

Low Risk: Indicates decreased risk of the fetus having conditions screened for.
High Risk: Suggests an increased likelihood that requires further diagnosis through tests such as amniocentesis or chorionic villus sampling (CVS).

It's well worth remembering that a high-risk result does not diagnose a condition; it merely indicates that further evaluation is required.

Related Tests

Depending upon specific situations, health care providers might recommend additional tests:

Prompt: Performed during the first trimester, where hCG and PAPP-A levels are measured.
Quadruple Marker Test: The Triple Test triplets (AFP, hCG, estriol) supplemented with inhibin A for enhanced risk assessment.
Non-Invasive Prenatal Testing (NIPT): Screens fetal DNA in mother's blood for chromosomal defects with high sensitivity.

These screens can further counsel and guide decisions.

Triple Marker Test is a significant aspect of prenatal screening, giving feedback on possible risk for some fetal conditions. Expectant parents through knowledge and utilization of this test are able to make informed decisions and prepare for interventions accordingly.

Your health and well-being are important to us at MaxAtHome, where you receive complete care during your pregnancy.