The Double Marker Test is a critical screening test performed during the first trimester of pregnancy to assess the risk of chromosomal abnormalities such as Down Syndrome. This non-invasive test measures free beta-hCG and PAPP-A levels in the mother’s blood to evaluate the baby’s genetic health. Recommended for all expectant mothers, especially those over 35 or with a family history of genetic conditions, the test provides peace of mind and helps in early diagnosis for better prenatal care.
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