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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 to obtain the report for the Leukodystrophy Gene Panel test is 21 days.

What are the prerequisites for the test Leukodystrophy Gene Panel

  • Patients must have a clinical suspicion of leukodystrophy based on symptoms and family history.
  • A blood or saliva sample is required for genetic testing.
  • Prior authorization may be required by insurance companies for coverage of the test.

What are the measure values for the test Leukodystrophy Gene Panel

  • ARSA Gene Analysis: Normal
  • ARSA Gene Analysis: Abnormal
  • ARSA Gene Analysis: Variant of Unknown Significance
  • ARSA Gene Analysis: Not Detected
  • ARSA Gene Analysis: Not Analyzed
  • ASPA Gene Analysis: Normal
  • ASPA Gene Analysis: Abnormal
  • ASPA Gene Analysis: Variant of Unknown Significance
  • ASPA Gene Analysis: Not Detected
  • ASPA Gene Analysis: Not Analyzed
  • GLB1 Gene Analysis: Normal
  • GLB1 Gene Analysis: Abnormal
  • GLB1 Gene Analysis: Variant of Unknown Significance
  • GLB1 Gene Analysis: Not Detected
  • GLB1 Gene Analysis: Not Analyzed

What does this test Leukodystrophy Gene Panel identify?

  • Leukodystrophy Gene Panel identifies mutations in genes associated with various types of leukodystrophy, a group of genetic disorders that affect the white matter of the brain.
  • The panel tests for mutations in genes such as ABCD1, ARSA, ASPA, GALC, GLB1, PLP1, and others that are known to cause specific types of leukodystrophy.
  • By analyzing these genes, the test can help diagnose the specific type of leukodystrophy a patient may have, which can guide treatment decisions and provide important information for genetic counseling.

Why is this test Leukodystrophy Gene Panel taken?

Leukodystrophy Gene Panel test is taken to diagnose various genetic disorders that affect the white matter of the brain, known as leukodystrophies. These disorders are caused by mutations in genes that are involved in the production and maintenance of myelin, a fatty substance that insulates nerve fibers in the brain and spinal cord.

The test analyzes a panel of genes associated with different types of leukodystrophies, such as Krabbe disease, metachromatic leukodystrophy, adrenoleukodystrophy, and Pelizaeus-Merzbacher disease. By identifying mutations in these genes, healthcare providers can confirm a diagnosis of a specific leukodystrophy and provide appropriate treatment and management strategies for the patient.

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