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Reports Within:

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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 Usher Syndrome Gene Panel test is 14 days.

What are the prerequisites for the test Usher Syndrome Gene Panel

  • Sample Type: DNA
  • Specimen Requirements: 2-5 mL whole blood in EDTA tube or 10 μg DNA extracted from blood
  • Shipping Requirements: Ship at room temperature
  • Turnaround Time: 3 weeks
  • Methodology: Next Generation Sequencing
  • Targeted Genes: MYO7A, USH1C, CDH23, PCDH15, USH1G, CIB2, USH2A, GPR98, DFNB31, CLRN1, HARS, PDZD7, WHRN, ADGRV1, and CACNA1D

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

  • USH1C Gene - 0.5x coverage
  • USH1G Gene - 0.7x coverage
  • CDH23 Gene - 0.6x coverage
  • MYO7A Gene - 0.8x coverage
  • PCDH15 Gene - 0.9x coverage

What does this test Usher Syndrome Gene Panel identify?

  • Usher Syndrome Gene Panel identifies mutations in genes associated with Usher syndrome, a genetic disorder characterized by hearing loss and progressive vision loss.
  • The panel includes analysis of genes such as MYO7A, USH2A, CDH23, PCDH15, and others that are known to be involved in Usher syndrome.
  • Identifying mutations in these genes can help in diagnosing Usher syndrome, determining the type and severity of the condition, and guiding treatment and management decisions.

Why is this test Usher Syndrome Gene Panel taken?

Usher Syndrome Gene Panel Test

The Usher Syndrome Gene Panel test is taken to diagnose Usher syndrome, a genetic disorder that affects both hearing and vision. This test analyzes specific genes known to be associated with Usher syndrome to identify any mutations that may be causing the condition.

Individuals with Usher syndrome typically experience hearing loss and progressive vision loss due to retinitis pigmentosa. By identifying the genetic mutations responsible for Usher syndrome, healthcare providers can provide a more accurate diagnosis, predict disease progression, and offer appropriate management and treatment options.

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