QUADRUPLE MARKER

4,935.00

Tests Details :

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Department : BIOCHEMISTRY

The Quadruple Marker test is a maternal blood screening test typically performed during the second trimester of pregnancy (usually between 15 to 20 weeks). It measures four substances in the mother’s blood: Alpha-fetoprotein (AFP), Human Chorionic Gonadotropin (hCG), Estriol (uE3), and Inhibin A.

These markers help assess the risk of chromosomal abnormalities such as Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and neural tube defects in the developing fetus.

This test does not provide a definitive diagnosis but indicates the likelihood of certain conditions.

The purpose of this test is to

  • To screen for chromosomal abnormalities
  • To assess risk of Down syndrome and Edwards syndrome
  • To detect risk of neural tube defects
  • To support prenatal screening
  • To guide further diagnostic evaluation

Tests Prepration :

Consult your doctor. No fasting is usually required Provide accurate details such as gestational age and maternal weight Inform your doctor about medical history Follow any specific instructions given by your healthcare provider
The Quadruple Marker test is a prenatal screening test that evaluates the risk of certain genetic and chromosomal abnormalities in the fetus.

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