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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 the report can be obtained for the test Congenital Stationary Night Blindness (CSNB) Gene Panel is 14 days.

What are the prerequisites for the test Congenital Stationary Night Blindness (CSNB) Gene Panel

  • Patients must have symptoms consistent with Congenital Stationary Night Blindness (CSNB)
  • Patients must have a family history of CSNB or related disorders
  • Patients must have a referral from a healthcare provider
  • Patients must provide informed consent for genetic testing

What are the measure values for the test Congenital Stationary Night Blindness (CSNB) Gene Panel

  • Panel Size: 5 genes
  • Genes Included: CABP4, CACNA1F, GPR179, NYX, TRPM1
  • Methodology: Next Generation Sequencing (NGS)
  • Turnaround Time: 3-4 weeks
  • Test Code: 2050

What does this test Congenital Stationary Night Blindness (CSNB) Gene Panel identify?

  • Congenital Stationary Night Blindness (CSNB) Gene Panel identifies genetic mutations in genes associated with CSNB, a rare inherited eye disorder that affects vision in low light conditions.
  • Specifically, this test looks for mutations in genes such as NYX, GRM6, TRPM1, and GPR179, which are known to be involved in the transmission of signals between photoreceptor cells and retinal neurons.
  • Identifying these mutations can help diagnose CSNB and guide treatment decisions for affected individuals.

Why is this test Congenital Stationary Night Blindness (CSNB) Gene Panel taken?

Why is this test Congenital Stationary Night Blindness (CSNB) Gene Panel taken?

The Congenital Stationary Night Blindness (CSNB) Gene Panel test is taken to identify genetic mutations associated with CSNB. CSNB is a hereditary eye disorder that affects the ability to see in low light conditions. By analyzing specific genes known to be linked to CSNB, this test can help diagnose the condition and guide treatment options. It is particularly important for individuals with a family history of CSNB or those experiencing symptoms such as difficulty seeing in dim light or night blindness.

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