The Double Marker test, also known as First Trimester Screening, is a vital prenatal blood test performed during pregnancy (usually between weeks 11 and 14). This test measures two specific markers in the mother’s blood: Free Beta-hCG and PAPP-A. Combined with an NT Scan (ultrasound), it helps assess the risk of chromosomal abnormalities, ensuring you have the information needed for a healthy pregnancy journey. 🛡️

Why should you take this test? 🤔

• Chromosomal Risk Assessment: Primarily screens for the risk of Down Syndrome (Trisomy 21) and Edwards Syndrome (Trisomy 18). 🏥

• Early Peace of Mind: Provides critical health insights during the first trimester, allowing for early medical guidance. ⏳

• Health Monitoring: Helps doctors monitor the developmental health of the fetus in the early stages. 👶

• Informed Decisions: Essential for expectant parents to understand potential genetic risks and plan accordingly with their healthcare provider. 📋

Test Specifications: 📋

• Sample Type: Blood (Serum) 🩸

• Preparation: No fasting required; however, it must be performed within a specific gestational window (11 to 13.6 weeks). 🗓️

• Requirement: An NT Scan (Ultrasound) report is mandatory to process the final risk calculation. 📑

• Reporting: High-precision screening results delivered within 2–3 days. ⏱️