KARYOTYPING FOR NEONATES BY G-BANDING / HEPARIN BLOOD

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Karyotyping for neonates by G-Banding is a genetic test performed on heparinized blood to analyze chromosomes for numerical or structural abnormalities. It helps in early detection of congenital chromosomal disorders such as Down syndrome, Turner syndrome, and other aneuploidies. This test is particularly useful for newborns with dysmorphic features, congenital anomalies, or abnormal prenatal screening results. Metropolis Healthcare uses advanced cytogenetic techniques to ensure accurate and reliable analysis for early intervention and clinical guidance

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Price: Rs. 4,770.00

Sample Type: HEPARIN BLOOD

Fasting Not Required


Booking Procedure:
  1. Technician from Metropolis will be assigned for a home sample collection after booking confirmation.
  2. Sample will be collected by our technician at your address at given slot.
  3. You can make the payment to the technician at the time of collection
  4. Your sample will then be transported to the nearest collection center and will be centrifuged before sending to the lab for processing.
  5. Soft copy reports will be sent to your email address within 24 to 48 hours or as per defined TAT for Tests.

Frequently Asked Questions (FAQ's):

What does neonatal karyotyping detect?
It identifies chromosomal abnormalities, including aneuploidies and structural rearrangements in newborns.

Who should undergo this test?
Newborns with congenital anomalies, dysmorphic features, or a family history of genetic disorders.

Is fasting required?
No fasting is required.

What sample is needed?
Heparinized blood collected via venipuncture.

How does Metropolis Healthcare perform this test?
Using G-Banding cytogenetic analysis to examine the neonate’s chromosomes for abnormalities.

Can this test detect all genetic disorders?
No, it detects chromosomal abnormalities but not single-gene mutations.

How long does it take to get results?
Results are typically available within 7–14 days depending on analysis complexity.

Why is early testing important in neonates?
Early detection allows timely clinical intervention, genetic counseling, and management planning

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