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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

Maximum Days for Report:

The report for the Stargardt Disease Gene Panel test can be obtained within 14-21 business days from the date of sample collection.

What are the prerequisites for the test Stargardt Disease Gene Panel

  • Patient must have suspected Stargardt Disease based on clinical presentation
  • Written informed consent from the patient or legal guardian
  • Complete requisition form with relevant clinical information
  • Previous genetic testing results, if available

What are the measure values for the test Stargardt Disease Gene Panel

  • ABCA4 Gene Sequencing: Normal
  • ABCA4 Gene Deletion/Duplication Analysis: Not Detected
  • PRPH2 Gene Sequencing: Normal
  • CNGB3 Gene Sequencing: Normal
  • CRX Gene Sequencing: Normal

What does this test Stargardt Disease Gene Panel identify?

  • Stargardt Disease Gene Panel identifies mutations in genes associated with Stargardt disease, a genetic disorder that causes progressive vision loss.
  • It specifically looks for mutations in genes such as ABCA4, ELOVL4, PROM1, and CNGB3, which are known to be involved in the development of Stargardt disease.
  • By identifying these mutations, the test can help in diagnosing Stargardt disease, predicting disease progression, and guiding personalized treatment options for affected individuals.

Why is this test Stargardt Disease Gene Panel taken?

Stargardt Disease Gene Panel Test

The Stargardt Disease Gene Panel test is taken to diagnose Stargardt disease, which is a type of inherited retinal disorder that causes progressive vision loss. This test specifically analyzes a panel of genes known to be associated with Stargardt disease, such as ABCA4, ELOVL4, PROM1, and others.

By identifying mutations in these genes, healthcare providers can confirm a diagnosis of Stargardt disease and provide appropriate treatment and management strategies for the patient. This test is particularly useful for individuals with a family history of Stargardt disease or those exhibiting symptoms of the condition, such as central vision loss, difficulty seeing in low light, and color vision abnormalities.

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