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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 to obtain the report for the Fraser Syndrome Gene Panel test is typically 10-14 business days. However, this time frame may vary depending on the laboratory and other factors.

What are the prerequisites for the test Fraser Syndrome Gene Panel

  • Patients suspected of Fraser syndrome based on clinical symptoms
  • Referral from a healthcare provider
  • Signed informed consent form

What are the measure values for the test Fraser Syndrome Gene Panel

  • Fraser Syndrome Gene Panel Test
  • Measure Values:
    • Gene Name: FRAS1
    • Gene Symbol: FRAS1
    • Chromosomal Location: 4q21.1
    • Test Type: Genetic Testing
    • Method: Next Generation Sequencing (NGS)
    • Test Sensitivity: >99%
    • Test Specificity: >99%
    • Turnaround Time: 3-4 weeks

What does this test Fraser Syndrome Gene Panel identify?

  • Fraser Syndrome Gene Panel is a genetic test that identifies mutations in genes associated with Fraser syndrome.
  • The test analyzes specific genes known to be involved in the development of Fraser syndrome, a rare genetic disorder characterized by abnormalities affecting the eyes, ears, nose, throat, and limbs.
  • By analyzing these genes, the test can help healthcare providers diagnose Fraser syndrome in individuals who exhibit symptoms of the disorder.
  • Identifying mutations in these genes can also help in providing genetic counseling to affected individuals and their families, as well as guiding treatment and management strategies.

Why is this test Fraser Syndrome Gene Panel taken?

Fraser Syndrome Gene Panel is taken to diagnose Fraser syndrome, a rare genetic disorder that affects the development of various parts of the body. This panel test is used to identify mutations in specific genes known to be associated with Fraser syndrome, such as FRAS1, FREM2, and GRIP1.

Individuals who exhibit symptoms of Fraser syndrome, such as cryptophthalmos (a condition where the eyelids are fused), syndactyly (webbed fingers or toes), and genitourinary abnormalities, may undergo this test to confirm the diagnosis and determine the underlying genetic cause.

Results from the Fraser Syndrome Gene Panel can help healthcare providers better understand the specific genetic mutations present in an individual with Fraser syndrome, which can inform treatment decisions and management strategies for the condition.

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