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CILIOPATHY GENE PANEL BY NGS, EDTA BLOOD

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NABL Cap Accredited 

This test uses advanced Next-Generation Sequencing to analyze genes associated with ciliopathies—genetic disorders caused by dysfunction of cellular cilia. It helps identify the underlying mutations responsible for multi-system conditions involving the kidneys, eyes, liver, brain, and skeletal system. Metropolis Healthcare provides high-quality sequencing and expert interpretation to support accurate diagnosis and clinical management. A blood sample collected in an EDTA vial is used for testing.

  • 17 Crores+ Samples Processed
  • World Class Technology Labs
  • 25+ Years of Trust & Experience
  • Free Home Collection

Price: Rs. 21,000.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes:G0174

Frequently Asked Questions (FAQ's):

What does the Ciliopathy Gene Panel include at Metropolis Healthcare?

It includes NGS-based analysis of multiple genes known to cause ciliopathy-related disorders.

 

How does Metropolis Healthcare perform this genetic test?
Metropolis Healthcare uses high-depth sequencing and bioinformatics to detect clinically significant genetic variants.

Who should take this test at Metropolis Healthcare?
Individuals with unexplained kidney disease, retinal disorders, skeletal anomalies, or suspected syndromic ciliopathies may benefit.

What sample is needed for this test at Metropolis Healthcare?
A blood sample collected in an EDTA tube is required for analysis.

How can this test help in diagnosis and management?
It helps confirm the genetic cause, guide treatment plans, and support long-term management strategies.

How long does Metropolis Healthcare take to provide results?
Report turnaround typically ranges from 2–4 weeks depending on analysis complexity.

Does this panel detect all known ciliopathy genes?
It covers the majority of established ciliopathy-associated genes, though extremely rare variants may need further evaluation.

Is genetic counseling recommended after this test at Metropolis Healthcare?
Yes, counseling helps interpret findings and understand inheritance patterns.

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