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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 test Alport Syndrome Gene Panel is 21 days.

What are the prerequisites for the test Alport Syndrome Gene Panel

  • Submission of a completed requisition form
  • Specimen types accepted include: whole blood in EDTA (purple top) tube
  • Patient must not be receiving therapy with high-dose biotin
  • Patient must not have received a heterologous blood transfusion within the last 6 months
  • Provide clinical information and family history

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

Gene Measure Value
COL4A3 Normal: 0-0.6
COL4A4 Normal: 0-0.6
COL4A5 Normal: 0-0.6

What does this test Alport Syndrome Gene Panel identify?

Alport Syndrome Gene Panel Test

The Alport Syndrome Gene Panel test is a genetic test that identifies mutations in specific genes associated with Alport Syndrome. Alport Syndrome is a genetic disorder that affects the kidneys, eyes, and ears. It is caused by mutations in genes involved in the production of type IV collagen, a key component of the basement membranes in these organs.

The Alport Syndrome Gene Panel test specifically looks for mutations in the COL4A3, COL4A4, and COL4A5 genes, which are known to be associated with Alport Syndrome. By identifying mutations in these genes, healthcare providers can confirm a diagnosis of Alport Syndrome and provide appropriate management and treatment for affected individuals.

Why is this test Alport Syndrome Gene Panel taken?

Alport Syndrome Gene Panel test is taken to diagnose Alport Syndrome, a genetic disorder that affects the kidneys and can lead to kidney failure. This test looks for mutations in certain genes that are associated with Alport Syndrome, including the COL4A3, COL4A4, and COL4A5 genes. By identifying these mutations, healthcare providers can confirm a diagnosis of Alport Syndrome and provide appropriate treatment and management options for the patient.

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