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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 the report can be obtained for the test Retinal Dysplasia Gene Panel is 21 days.

What are the prerequisites for the test Retinal Dysplasia Gene Panel

  • Sample Type: Blood (EDTA)
  • Sample Volume: 3-5 mL
  • Shipping Conditions: Ship at room temperature
  • Turnaround Time: 2-4 weeks
  • Test Code: 9001

What are the measure values for the test Retinal Dysplasia Gene Panel

  • Retinal Dysplasia Gene Panel
    • Measure Values:
    • 1. RDH12 Gene Mutation Analysis
    • 2. GUCY2D Gene Mutation Analysis
    • 3. CRB1 Gene Mutation Analysis
    • 4. RPGRIP1 Gene Mutation Analysis
    • 5. RPE65 Gene Mutation Analysis
    • 6. LRAT Gene Mutation Analysis
    • 7. AIPL1 Gene Mutation Analysis

What does this test Retinal Dysplasia Gene Panel identify?

  • Retinal Dysplasia Gene Panel identifies mutations in genes associated with retinal dysplasia, a group of genetic disorders that affect the development and function of the retina.
  • These mutations can cause abnormalities in the structure and function of the retina, leading to visual impairment or blindness.
  • The panel tests for mutations in genes such as RPE65, CRB1, and RPGR, which are known to be associated with retinal dysplasia.
  • Identification of these mutations can help in making an accurate diagnosis of retinal dysplasia and guiding appropriate treatment and management strategies.

Why is this test Retinal Dysplasia Gene Panel taken?

Retinal Dysplasia Gene Panel Test

The Retinal Dysplasia Gene Panel Test is taken to identify mutations in genes associated with retinal dysplasia, a group of eye disorders that affect the development of the retina. Retinal dysplasia can lead to vision problems and blindness in affected individuals.

By analyzing the genetic makeup of an individual using this panel test, healthcare providers can determine the presence of mutations that may be causing retinal dysplasia. This information can help in diagnosing the condition, predicting its progression, and guiding treatment decisions.

Early detection of genetic mutations associated with retinal dysplasia through this test can also aid in genetic counseling for affected individuals and their families. Understanding the underlying genetic cause of the condition can assist in making informed decisions about family planning and potential risk of passing on the condition to future generations.

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