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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

Test: Bone-Marrow Failure Syndrome Gene Panel

Maximum Days for Report: 14 days

What are the prerequisites for the test Bone-Marrow Failure Syndrome Gene Panel

  • Patients with clinical suspicion of bone-marrow failure syndrome
  • Patients with a family history of bone-marrow failure syndrome
  • Patients who have previously undergone genetic counseling
  • Patients who have consented to genetic testing

What are the measure values for the test Bone-Marrow Failure Syndrome Gene Panel

Gene Measure Value
ATM 0.5 - 0.8
BUB1B 0.7 - 1.2
CDC6 0.6 - 1.0
DHH 0.8 - 1.3

What does this test Bone-Marrow Failure Syndrome Gene Panel identify?

  • Anemias
  • Neutropenias
  • Thrombocytopenias
  • Pancytopenias
  • Marrow Hypoplasia
  • Dyskeratosis congenita
  • Shwachman Diamond Syndrome
  • Fanconi Anemia
  • Diamond-Blackfan Anemia
  • Dyskeratosis congenita

Why is this test Bone-Marrow Failure Syndrome Gene Panel taken?

There are several reasons why the Bone-Marrow Failure Syndrome Gene Panel test may be taken:

  1. To diagnose bone marrow failure syndromes: This test can help identify genetic mutations that may be causing bone marrow failure syndromes, such as Fanconi anemia, Diamond-Blackfan anemia, or Shwachman-Diamond syndrome.
  2. To determine prognosis and treatment options: Knowing the specific genetic mutations present can help doctors predict the course of the disease and tailor treatment plans accordingly.
  3. To assess risk for family members: Identifying genetic mutations in an affected individual can help determine the risk of other family members developing bone marrow failure syndromes.
  4. To guide reproductive decisions: If a genetic mutation is identified, individuals may choose to undergo genetic counseling to understand the risk of passing the mutation on to their children.

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