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Reports Within:

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Requisites
Measures

Number of red blood cells in the blood

Identifies

Red blood cell disorders

Measures: Number of red blood cells in the blood

Identifies: Red blood cell disorders

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What is the maximum days the report can be obtained for the test

Test: Osteogenesis Imperfecta Gene Panel

Maximum Days to Obtain Report: 21 days

What are the prerequisites for the test Osteogenesis Imperfecta Gene Panel

  • Patients with suspected Osteogenesis Imperfecta based on clinical symptoms
  • Referral from a healthcare provider
  • Consent form signed by the patient or guardian
  • Insurance pre-authorization if required

What are the measure values for the test Osteogenesis Imperfecta Gene Panel

  • COL1A1 Gene Sequencing: $500
  • COL1A2 Gene Sequencing: $500
  • COL1A1 and COL1A2 Gene Sequencing: $900
  • COL1A1 Gene Deletion/Duplication Analysis: $600
  • COL1A2 Gene Deletion/Duplication Analysis: $600
  • COL1A1 and COL1A2 Gene Deletion/Duplication Analysis: $1000

What does this test Osteogenesis Imperfecta Gene Panel identify?

  • Osteogenesis Imperfecta Gene Panel identifies mutations in genes associated with Osteogenesis Imperfecta, a group of genetic disorders characterized by fragile bones that break easily.
  • This panel helps in diagnosing Osteogenesis Imperfecta and determining the specific genetic cause of the condition in an individual.
  • Genes included in this panel may include COL1A1, COL1A2, CRTAP, LEPRE1, P3H1, and others that are known to be related to Osteogenesis Imperfecta.
  • Identifying mutations in these genes can help in providing personalized treatment and management strategies for individuals with Osteogenesis Imperfecta.

Why is this test Osteogenesis Imperfecta Gene Panel taken?

This test is taken to diagnose Osteogenesis Imperfecta, a genetic disorder characterized by fragile bones that break easily. It is caused by mutations in genes that are involved in the production of collagen, a protein that provides strength and structure to bones. The Osteogenesis Imperfecta Gene Panel helps to identify specific genetic mutations that are associated with the condition, allowing for an accurate diagnosis and appropriate treatment plan to be developed.

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