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OSTEOGENESIS IMPERFECTA GENE PANEL BY NGS, EDTA BLOOD

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NABL Cap Accredited 

The Osteogenesis Imperfecta Gene Panel by NGS is a focused genetic test designed to detect mutations associated with various types of osteogenesis imperfecta, a group of inherited bone fragility disorders. Metropolis Healthcare uses advanced Next-Generation Sequencing (NGS) to analyze multiple collagen-related and bone-formation genes. This test helps confirm diagnosis, determine disease severity, and guide clinical management and family counseling. It is especially useful for individuals with recurrent fractures, bone deformities, or a family history of brittle bone disease. 

  • 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:G0234

Frequently Asked Questions (FAQ's):

What does the Osteogenesis Imperfecta Gene Panel include?
It includes detailed gene sequencing performed by Metropolis Healthcare to identify mutations linked to brittle bone disorders.

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

Who should take this test?
Individuals with frequent fractures, bone deformities, blue sclera, or a family history of osteogenesis imperfecta may benefit.

Can this test determine the type of osteogenesis imperfecta?
Yes, the panel helps identify the genetic subtype, supporting accurate diagnosis and prognosis assessment.

What sample is required for this test?
An EDTA blood sample is used for DNA extraction and genetic sequencing.

Is this test useful for family planning and counseling?
Yes, it helps determine carrier status and inheritance risks, guiding informed reproductive decisions.

How long does Metropolis Healthcare take to provide results?
Results typically take a few weeks due to in-depth sequencing and expert analysis.

Does this test help guide treatment or management?
While treatment is supportive, genetic confirmation helps tailor monitoring, therapy planning, and long-term care strategies

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