Double Marker Test Explained: Early Screening for Chromosomal Abnormalities
To detect chromosomal abnormalities, a screening test is done in the 11th and 13th weeks of pregnancy. It is called a double marker test. This test evaluates the levels of:
1. Free Beta hCG (Human Chorionic Gonadotropin): This hormone is produced by the placenta during pregnancy. Elevated levels may indicate chromosomal risks.
2. PAPP-A (Pregnancy-Associated Plasma Protein-A): This protein is produced by the placenta to maintain its health. Low levels may indicate placental issues or chromosomal disorders.
The test offers several benefits as it plays a vital role in the early pregnancy care for several reasons:
Non-Invasive: Since it is a normal blood test, it does not pose any risk to the baby or mother.
Early Detection: With the early identification of genetic abnormalities, the doctor can suggest additional diagnostic tests, such as amniocentesis or CVS, for a more conclusive diagnosis.
Reassurance: Getting insights into the baby’s genetic health helps reduce parental anxiety.
If you live in Delhi-NCR, you can do an online search with keywords double marker test price, to find out the best diagnostic centres in your vicinity.
Disclaimer: This information is meant for general reference only. For personalised advice, always consult your physician or a qualified healthcare professional.

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