Royal Health Group

Double Marker

The Double Marker Test is a common prenatal screening test used to identify the risk of certain chromosomal abnormalities in a developing fetus, specifically Down syndrome (trisomy 21) and Trisomy 18. It is mostly performed during the first trimester, usually between the 9th and 13th weeks of pregnancy.

 

Double Marker Test

Benefits of Double Marker

One phone call for a better health

  • Early Risk Detection: Identifies potential risks for Down syndrome and Trisomy 18 in the first trimester.
  • Non-Invasive Procedure: Safe blood test with no risk to the fetus.
  • Guides Further Testing: Helps determine the need for additional diagnostic tests (e.g., CVS, amniocentesis).
  • Peace of Mind: A low risk result offers reassurance to expectant parents.
  • Informed Decision Making: Enables parents to make well informed choices about further testing or interventions.
  • Comprehensive Assessment: Considers factors like PAPP-A, hCG, maternal age, and medical history.
  • Accessible and Affordable: More accessible and affordable than invasive tests.
  • Early Intervention Planning: Helps parents plan for potential early interventions or special needs if necessary.

FAQ's

FREQUENTLY ASKED QUESTIONS

The Double Marker Test is generally offered to all pregnant women, but it’s especially useful for those who are at a higher risk of chromosomal abnormalities. This includes women over 35, those with a family history of genetic conditions, or women who have had previous pregnancies with chromosomal abnormalities.

For getting Double Marker Test at home . Call Royal Health Group Home Care on +971 50 844 3803 

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