What is Double Marker Test?
The Double Marker Test, also known as the Dual Marker Test or the First Trimester Screening Test, is a prenatal screening test designed to assess the risk of certain chromosomal abnormalities and genetic disorders in the developing fetus. This test is typically performed between 10 to 13 weeks of pregnancy and combines the measurement of two specific substances in the mother’s blood with an ultrasound measurement of the thickness of the baby’s neck.
Advantages
Early Detection: The test can be performed during the first trimester, providing you with early insights into the health of your baby.
Non-Invasive: The Double Marker Test is a safe and non-invasive procedure that carries no risk to you or your baby.
Risk Assessment: By analyzing specific markers and combining them with relevant factors, our experts can estimate the risk of chromosomal abnormalities accurately.
Personalized Consultation: Our compassionate team of genetic counselors will interpret the test results and guide you through the process, addressing any concerns you may have.
Conclusion
It’s important to note that the Double Marker Test is a screening test and not a diagnostic test. If the results indicate an increased risk of chromosomal abnormalities, further diagnostic tests, such as amniocentesis or chorionic villus sampling (CVS), may be recommended to confirm the findings.
Schedule an Appointment
At Jogal Women’s Hospital, we prioritize your comfort and convenience throughout the entire testing process. Our dedicated staff will ensure that you receive comprehensive care, from the moment you arrive for your appointment to the delivery of your test results.
Choose Jogal Women’s Hospital for advanced prenatal care and trusted expertise. Your well-being and the health of your baby are our top priorities.
