Description
Why It’s Done:
The Dual Marker Test is used to evaluate the risk of certain genetic and chromosomal conditions in the fetus, including:
• Down syndrome (Trisomy 21)
• Trisomy 18 (Edwards syndrome)
• Other rare chromosomal abnormalities
Preparation:
• No special preparation or fasting is required.
• The test involves a blood sample from the mother’s arm.
• It is usually done along with a nuchal translucency ultrasound.
• Accurate dating of pregnancy (gestational age) is important for reliable results, so your doctor may suggest an ultrasound beforehand.


