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POLYCYSTIC KIDNEY DISEASE GENE PANEL BY NGS, EDTA BLOOD

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NABL Cap Accredited 

The Polycystic Kidney Disease Gene Panel by NGS is a focused genetic test designed to detect mutations linked to autosomal dominant and autosomal recessive forms of polycystic kidney disease (PKD). Metropolis Healthcare uses advanced Next-Generation Sequencing (NGS) to analyze multiple kidney-related genes to support accurate diagnosis and risk assessment. This test helps identify the genetic cause of cystic kidney enlargement, hypertension, and progressive renal dysfunction. It is particularly valuable for individuals with kidney cysts, family history of PKD, or early-onset renal symptoms. 

  • 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


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 the Polycystic Kidney Disease Gene Panel include?
It includes detailed genetic sequencing performed by Metropolis Healthcare to detect mutations associated with PKD.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses high-resolution NGS platforms to analyze genes responsible for kidney cyst formation from an EDTA blood sample.

Who should take this test?
Individuals with kidney cysts, early kidney dysfunction, or a family history of polycystic kidney disease may benefit.

Can this test distinguish between ADPKD and ARPKD?
Yes, the panel helps differentiate between autosomal dominant and autosomal recessive PKD by identifying specific gene mutations.

What sample is required for this test?
An EDTA blood sample is required for DNA extraction and comprehensive gene analysis.

Is this test useful for family planning and counseling?
Yes, identifying the causative mutation helps determine inheritance risks and supports genetic counseling for families.

How long does Metropolis Healthcare take to deliver results?
Results generally take a few weeks due to detailed sequencing and interpretation.

Does this test guide treatment or management?
While it does not alter treatment directly, genetic confirmation helps clinicians monitor complications, plan interventions, and guide long-term kidney care.

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