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Reports Within

Parameters

Reports Within:

Parameter Include:

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

Maximum days to obtain the report for the Osteopetrosis Gene Panel test: 30 days

What are the prerequisites for the test Osteopetrosis Gene Panel

  • Patients with symptoms or a family history suggestive of osteopetrosis
  • Patients with a suspected diagnosis of osteopetrosis
  • Patients with a known family mutation for osteopetrosis

What are the measure values for the test Osteopetrosis Gene Panel

  • ALPL Gene Sequencing and Deletion/Duplication Analysis - Reported as:
    • ALPL Gene Sequencing:
    • Deletion/Duplication Analysis:
  • CLCN7 Gene Sequencing and Deletion/Duplication Analysis - Reported as:
    • CLCN7 Gene Sequencing:
    • Deletion/Duplication Analysis:
  • CA2 Gene Sequencing and Deletion/Duplication Analysis - Reported as:
    • CA2 Gene Sequencing:
    • Deletion/Duplication Analysis:

What does this test Osteopetrosis Gene Panel identify?

  • Osteopetrosis Gene Panel identifies mutations in genes associated with osteopetrosis, a rare genetic disorder characterized by abnormal bone growth and density.
  • Some of the genes included in this panel are: TCIRG1, CLCN7, PLEKHM1, SNX10, OSTM1, and others.
  • The test helps in diagnosing osteopetrosis and determining the specific genetic cause of the condition in an individual.
  • Identifying mutations in these genes can aid in genetic counseling, family planning, and personalized treatment strategies for individuals with osteopetrosis.

Why is this test Osteopetrosis Gene Panel taken?

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Osteopetrosis Gene Panel is taken to diagnose and confirm the presence of osteopetrosis, a rare genetic disorder that affects bone development and leads to abnormally dense bones. This test helps in identifying mutations in specific genes that are known to cause different types of osteopetrosis. Early detection and diagnosis of osteopetrosis through genetic testing can help in determining appropriate treatment options, monitoring disease progression, and providing genetic counseling to affected individuals and their families.

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