Double Marker test Near Me in Noida

It is used to screen for chromosomal abnormalities like Down Syndrome and Edward’s Syndrome in the fetus during the first trimester of pregnancy.

The test is recommended between 8 to 14 weeks of gestation.

Fasting is generally not required, but follow your doctor’s instructions if additional tests are ordered.

Results are typically available within 4 days after sample collection.

An abnormal result indicates a higher risk of abnormalities. Consult your doctor for further tests, such as an NT scan or amniocentesis, for confirmation.

The test is typically performed between 11 and 14 weeks of pregnancy, usually alongside the Nuchal Translucency (NT) scan.

Yes, it is a non-invasive screening test that only requires a blood sample from the mother. It poses no risk to the fetus.

No, the Double Marker Test is a screening test, not a diagnostic one. It estimates the risk of chromosomal abnormalities. If the result is high-risk, your doctor may recommend further confirmatory tests such as NIPT, CVS, or amniocentesis.

The test is considered highly reliable when combined with NT scan results. It can detect a significant percentage of chromosomal abnormalities but may require follow-up testing for confirmation.

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