TRISOMY (ANEUPLOIDY) FOR CHROMOSOME (18, X & Y) / HEPARIN BLOOD

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The Trisomy (Aneuploidy) test for Chromosomes 18, X, and Y using heparin blood helps detect abnormal chromosome numbers in individuals being evaluated for genetic conditions. It is useful when chromosomal analysis is required postnatally or in specific clinical situations. Metropolis Healthcare performs this test using advanced molecular and cytogenetic technologies for accurate chromosomal detection. The results assist clinicians in diagnosing genetic abnormalities and guiding appropriate medical management

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Price: Rs. 5,620.00

Sample Type: HEPARIN BLOOD

Fasting Not Required


Notes: T0124

Frequently Asked Questions (FAQ's):

What does the Trisomy (Aneuploidy) test for Chromosomes 18, X & Y include at Metropolis Healthcare?
It includes detailed chromosomal analysis of heparinized blood to detect extra or missing copies of chromosomes 18, X, and Y.

How does Metropolis Healthcare perform this chromosomal test?
The lab uses advanced cytogenetic and molecular techniques to ensure precise identification of aneuploidies.

Who should consider this test at Metropolis Healthcare?
Individuals with clinical features suggestive of chromosomal disorders or those needing confirmatory genetic evaluation may benefit from this test.

Why is this aneuploidy test important at Metropolis Healthcare?
It helps diagnose key chromosomal abnormalities, enabling timely medical guidance and follow-up care.

Is any preparation required for this heparin blood test at Metropolis Healthcare?
No special preparation is needed; a heparinized blood sample is collected for analysis.

How soon are results available from Metropolis Healthcare?
Results are typically delivered within the standard turnaround time for chromosomal studies.

What do abnormal findings mean in a Metropolis Healthcare report?
Abnormalities may indicate trisomy or sex chromosome variations and should be reviewed with a genetic specialist.

Can this test be combined with other genetic evaluations at Metropolis Healthcare?
Yes, it can be paired with karyotyping, microarray, or broader aneuploidy panels for comprehensive genetic assessment.

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