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Reports Within

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 Cardiomyopathy Gene Panel is 21 days.

What are the prerequisites for the test Cardiomyopathy Gene Panel

  • Written informed consent
  • Completed test requisition form
  • Family history documentation
  • Copy of relevant medical records
  • Payment information

What are the measure values for the test Cardiomyopathy Gene Panel

  • Gene 1: 3.5
  • Gene 2: 2.1
  • Gene 3: 4.8
  • Gene 4: 1.9
  • Gene 5: 3.2

What does this test Cardiomyopathy Gene Panel identify?

This test identifies mutations in genes associated with various types of cardiomyopathy, including:

  • Hypertrophic cardiomyopathy
  • Dilated cardiomyopathy
  • Arrhythmogenic right ventricular cardiomyopathy
  • Restrictive cardiomyopathy

Why is this test Cardiomyopathy Gene Panel taken?

Reason for Cardiomyopathy Gene Panel Test

Reason for Test:

The Cardiomyopathy Gene Panel test is taken to assess certain genetic mutations that may be associated with cardiomyopathy, a condition that affects the heart muscle. Cardiomyopathy can lead to various symptoms such as shortness of breath, fatigue, chest pain, and irregular heartbeats. Identifying specific genetic mutations through this panel test can help in determining the underlying cause of cardiomyopathy in an individual.

By identifying genetic mutations, healthcare providers can better manage and treat cardiomyopathy, as well as provide personalized treatment plans based on the individual's genetic profile. Additionally, this test can help in identifying family members who may be at risk of developing cardiomyopathy due to inherited genetic mutations.

Overall, the Cardiomyopathy Gene Panel test plays a crucial role in the diagnosis, treatment, and management of cardiomyopathy by providing valuable genetic information that can guide healthcare decisions and improve patient outcomes.

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