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


Notes: K0030

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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