TRISOMY (ANEUPLOIDY) FOR CHROMOSOME (13, 18, 21, X, Y) / CORD BLOOD

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NABL Cap Accredited      
This test examines chromosomes 13, 18, 21, X, and Y in cord blood to detect common aneuploidies. It helps identify genetic conditions such as Down syndrome, Edwards syndrome, Patau syndrome, and sex chromosome abnormalities after birth. Cord blood offers a reliable source of fetal cells for accurate chromosomal evaluation. The results assist clinicians in confirming diagnoses and planning further care 

  • 17 Crores+ Samples Processed
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Price: Rs. 9,330.00

Sample Type: CORD BLOOD

Fasting Not Required

Notes: T0121

Frequently Asked Questions (FAQ's):

What does this test detect?
It identifies aneuploidies involving chromosomes 13, 18, 21, X, and Y.

Why is cord blood used for this test?
Cord blood offers newborn-derived cells that help ensure precise chromosomal analysis.

What conditions can this test confirm?
It can confirm disorders like Down syndrome, Edwards syndrome, Patau syndrome, Turner syndrome, and Klinefelter syndrome.

How is the analysis performed?
Techniques such as PCR, FISH, or karyotyping may be used depending on the laboratory.

How long does it take to get the report?

Reports are typically available within 5–10 working days. 

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Free Sample Pickup from Home/Office

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Need help? Call +91-8595219293

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  1. Appointment confirmation and Technician details will be provided to you Through Email & SMS well in advance.
  2. The date and time of collection may change if Technicians are not available at the requested time.
  3. Kindly allow 30 minutes (Plus or Minus)for the technician to find and reach your location through possible traffic/weather.

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