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Reports Within

Parameters

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

The maximum days for obtaining the report for the Fanconi Anemia Gene Panel test is 14 days.

What are the prerequisites for the test Fanconi Anemia Gene Panel

  • Patients must have a suspected diagnosis of Fanconi Anemia based on clinical symptoms and family history.
  • Patients must have a referral from a qualified healthcare provider such as a genetic counselor, hematologist, or oncologist.
  • Prior to testing, patients must provide informed consent for genetic testing and counseling.
  • Patients should have blood samples collected for DNA extraction and analysis.
  • Patients may need to undergo additional confirmatory testing such as bone marrow biopsy or chromosome breakage analysis.

What are the measure values for the test Fanconi Anemia Gene Panel

Gene Measure Value
FANCA >99% sensitivity, >99% specificity
FANCB >99% sensitivity, >99% specificity
FANCC >99% sensitivity, >99% specificity
FANCD2 >99% sensitivity, >99% specificity
FANCE >99% sensitivity, >99% specificity

What does this test Fanconi Anemia Gene Panel identify?

The Fanconi Anemia Gene Panel is a test that identifies mutations in genes associated with Fanconi Anemia, a rare genetic disorder that affects bone marrow function and increases the risk of certain cancers.

  • BRCA2
  • BRIP1
  • FANCA
  • FANCB
  • FANCC
  • FANCD2
  • FANCE
  • FANCF
  • FANCG
  • FANCI
  • FANCL
  • FANCM
  • PALB2

Why is this test Fanconi Anemia Gene Panel taken?

Fanconi Anemia Gene Panel is taken to diagnose Fanconi anemia, a rare genetic disorder that affects the bone marrow and leads to bone marrow failure, increased risk of cancer, and other serious health problems. This test helps identify mutations in the genes associated with Fanconi anemia, allowing for early detection and appropriate management of the condition. It is often recommended for individuals with a family history of Fanconi anemia or those showing symptoms of the disorder, such as abnormal blood counts, birth defects, and developmental delays.

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