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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 the report can be obtained for the test Dyskeratosis Congenita Gene Panel is 30 days.

What are the prerequisites for the test Dyskeratosis Congenita Gene Panel

  • Requisition form with patient information
  • Consent form signed by the patient or legal guardian
  • Complete clinical history of the patient
  • Family history of dyskeratosis congenita or related disorders
  • Results of any previous genetic testing, if available
  • Payment information or insurance details

What are the measure values for the test Dyskeratosis Congenita Gene Panel

  • DKC1 Gene Analysis: Sequencing and Deletion/Duplication
  • TERC Gene Analysis: Sequencing and Deletion/Duplication
  • TERT Gene Analysis: Sequencing and Deletion/Duplication

What does this test Dyskeratosis Congenita Gene Panel identify?

  • Dyskeratosis Congenita Gene Panel identifies mutations in genes associated with dyskeratosis congenita, a rare inherited disorder that affects multiple body systems.
  • The panel includes analysis of genes such as DKC1, TERT, TERC, and RTEL1, which play a role in maintaining telomere length and function.
  • Identification of mutations in these genes can help confirm a diagnosis of dyskeratosis congenita and guide treatment decisions.
  • Early detection of mutations through genetic testing can also help with family planning and provide information on the risk of passing the condition to future generations.

Why is this test Dyskeratosis Congenita Gene Panel taken?

The Dyskeratosis Congenita Gene Panel test is taken to diagnose Dyskeratosis Congenita, a rare genetic disorder that affects multiple organ systems. This test helps in identifying mutations in specific genes associated with Dyskeratosis Congenita, such as DKC1, TERT, TERC, and others.

Early diagnosis of Dyskeratosis Congenita is important as it can help in providing appropriate medical management and monitoring to prevent complications associated with the disorder. The test results can also help in genetic counseling for affected individuals and their families.

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