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PACHYDERMOPERIOSTOSIS & PRIMARY HYPERTROPHIC OSTEOARTHROPATHY GENE PANEL BY NGS, EDTA BLOOD

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NABL Cap Accredited 

The Pachydermoperiostosis & Primary Hypertrophic Osteoarthropathy Gene Panel by NGS is a specialized test designed to detect genetic mutations associated with these rare disorders affecting skin thickening, bone growth, and joint changes. Metropolis Healthcare uses advanced Next-Generation Sequencing (NGS) to analyze multiple genes linked to abnormal bone and connective tissue development. This panel supports accurate diagnosis, helps differentiate primary from secondary forms, and guides long-term management. It is especially helpful for individuals with clubbing, joint pain, coarse facial features, or a family history of these conditions. 

  • 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:G0236

Frequently Asked Questions (FAQ's):

What does this gene panel include?
It includes detailed sequencing conducted by Metropolis Healthcare to detect mutations linked to pachydermoperiostosis and primary hypertrophic osteoarthropathy.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses high-precision NGS to analyze disease-associated genes from an EDTA blood sample.

Who should consider taking this test?
Individuals with digital clubbing, skin thickening, excessive sweating, or unexplained joint changes may benefit.

Can this test confirm the type of hypertrophic osteoarthropathy?
Yes, it helps differentiate primary genetic forms from secondary causes related to other illnesses.

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

Is this test useful for family counseling?
Yes, identifying the mutation helps clarify inheritance risks and supports genetic counseling for family members.

How long does Metropolis Healthcare take to provide results?
Results usually take a few weeks due to extensive sequencing and interpretation.

Does this test guide treatment or management?

While treatment is mainly supportive, genetic confirmation helps clinicians personalize care and monitor long-term complications. 

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