FIRST TRIMESTER SCREENING (FTS)

Combines two maternal blood markers and an early ultrasound to estimate risk of fetal chromosomal problems in Visit Clinic.
What is a FIRST TRIMESTER SCREENING (FTS) Test in Visit Clinic?
First trimester screening measures specific substances in the mother's blood and an early ultrasound measurement. The blood tests look at PAPP-A and free beta hCG. The ultrasound measures nuchal translucency at about 11 to 13 weeks and 6 days. These results, combined with maternal age and pregnancy dating, estimate the chance of chromosomal conditions such as Down syndrome and Trisomy 18. It gives a risk estimate, not a diagnosis. Doctors use the result to guide counseling and decide if further testing like cell-free DNA screening or diagnostic testing is needed.
FIRST TRIMESTER SCREENING (FTS) Test Preparation in Visit Clinic
No special preparation is required.
FIRST TRIMESTER SCREENING (FTS) Test Parameters in Visit Clinic
The FIRST TRIMESTER SCREENING (FTS) test evaluates various parameters. Here are the main parameters checked:
Why Take a FIRST TRIMESTER SCREENING (FTS) Test in Visit Clinic?
FIRST TRIMESTER SCREENING (FTS) is typically done as a combined panel of maternal blood markers and an early ultrasound. Clinicians order it for routine prenatal risk assessment, for older maternal age, or after an abnormal scan. It helps identify increased risk for chromosomal conditions such as Down syndrome and Trisomy 18. Abnormal results can arise from dating errors, multiple pregnancy, maternal factors, or true fetal problems, and a family history of chromosomal conditions makes the test especially relevant.
Search by test names and add it to your cart

Choose your preferred labs from top trusted partners

Select a convenient date and time for your test

Make payment and get confirmation within 2 hours

For any unanswered questions, reach out to our support team via email. We will assist you as soon as possible