The double marker test is a prenatal screening tool used to assess the risk of chromosomal abnormalities such as Down syndrome in the developing fetus. This double marker test measures specific markers in the mother's blood and is usually performed in the first trimester of pregnancy. The results, combined with an ultrasound, provide a risk assessment for chromosomal disorders. Early detection through double marker testing allows for informed decision-making and timely medical intervention, ensuring the health and well-being of both the mother and the baby.

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