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Parameters

Reports Within:

Parameter Include:

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 Myotonic Dystrophy For ZFN9 Gene Test is typically 14-21 business days from the date of sample collection.

What are the prerequisites for the test Myotonic Dystrophy For ZFN9 Gene Test

  • Valid doctor's prescription
  • Signed informed consent form
  • Completed test requisition form
  • Specimen collection kit
  • Patient demographic information
  • Insurance information (if applicable)

What are the measure values for the test Myotonic Dystrophy For ZFN9 Gene Test

Test Name:
Myotonic Dystrophy For ZFN9 Gene Test
Measure Values:
  • Normal: Less than 35 CTG repeats
  • Intermediate: 35-49 CTG repeats
  • Full mutation: 50 or more CTG repeats

What does this test Myotonic Dystrophy For ZFN9 Gene Test identify?

  • This test specifically identifies the ZFN9 gene associated with Myotonic Dystrophy.
  • It helps in determining the presence of genetic mutations in the ZFN9 gene, which are linked to Myotonic Dystrophy.
  • The test results provide information on the potential risk of developing Myotonic Dystrophy based on the genetic profile of the individual.
  • It can help in early diagnosis and management of Myotonic Dystrophy by identifying individuals who may be at a higher risk for the condition.

Why is this test Myotonic Dystrophy For ZFN9 Gene Test taken?

Myotonic Dystrophy For ZFN9 Gene Test is taken to diagnose Myotonic Dystrophy, a genetic disorder that affects muscle function and can cause muscle weakness and wasting, as well as other symptoms such as cataracts, heart problems, and cognitive impairment. The ZFN9 gene test specifically looks for mutations in the ZNF9 gene, which is associated with Myotonic Dystrophy type 2. Identifying mutations in this gene can help confirm a diagnosis of Myotonic Dystrophy and guide treatment and management decisions.

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