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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

Maximum Report Turnaround Time for Deafness Gene Panel Test:

The report for the Deafness Gene Panel test can be obtained within 14-21 business days from the date of sample receipt at the testing facility.

What are the prerequisites for the test Deafness Gene Panel

  • Completion of the test requisition form
  • Submission of a blood sample from the patient
  • Documentation of the patient's medical history and family history of hearing loss
  • Confirmation of payment or insurance coverage for the test

What are the measure values for the test Deafness Gene Panel

Gene Measure Value
GJB2 Positive/Negative
GJB6 Positive/Negative
MYO7A Positive/Negative
OTOA Positive/Negative

What does this test Deafness Gene Panel identify?

  • The test Deafness Gene Panel identifies mutations in genes associated with both syndromic and non-syndromic forms of deafness.
  • Syndromic forms of deafness refer to hearing loss that is accompanied by other medical conditions or physical abnormalities, while non-syndromic forms of deafness involve isolated hearing loss without other associated symptoms.
  • The panel typically includes analysis of genes such as GJB2, SLC26A4, and CDH23, among others, which are known to be involved in the development and function of the inner ear and auditory system.
  • Identifying mutations in these genes can help diagnose the underlying cause of deafness in an individual, determine the inheritance pattern of the condition, and guide appropriate management and treatment options.

Why is this test Deafness Gene Panel taken?

The Deafness Gene Panel test is taken to identify mutations in genes that are associated with hearing loss. This test is usually recommended for individuals who have a family history of deafness or hearing loss, or for those who are experiencing hearing loss at a young age. By identifying specific genetic mutations, healthcare providers can determine the cause of the hearing loss and provide appropriate treatment and management strategies.

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