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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 for obtaining the report for the Ehlers Danlos Syndrome (EDS) Gene Panel test is typically 14-21 days. However, the exact time frame may vary depending on the specific laboratory conducting the test and other factors such as sample processing and analysis.

What are the prerequisites for the test Ehlers Danlos Syndrome (EDS) Gene Panel

  • Referral from a qualified healthcare provider
  • Confirmation of clinical diagnosis of Ehlers Danlos Syndrome
  • Consent form signed by the patient or legal guardian
  • Insurance pre-authorization if applicable

What are the measure values for the test Ehlers Danlos Syndrome (EDS) Gene Panel

Gene Measure Value
COL1A1 0-2 variants detected
COL1A2 0-2 variants detected
C1R 0-1 variants detected
C1S 0-1 variants detected

What does this test Ehlers Danlos Syndrome (EDS) Gene Panel identify?

  • Ehlers Danlos Syndrome (EDS) Gene Panel identifies mutations in genes associated with various types of Ehlers Danlos Syndrome, a group of connective tissue disorders characterized by joint hypermobility, skin hyperextensibility, and tissue fragility.
  • The panel typically includes genes such as COL5A1, COL5A2, COL1A1, COL1A2, COL3A1, TNXB, and others that are known to be involved in the synthesis and structure of collagen, a key component of connective tissues.
  • Identifying mutations in these genes can help confirm a diagnosis of EDS and provide information about the specific type and severity of the condition, which can guide treatment and management strategies.

Why is this test Ehlers Danlos Syndrome (EDS) Gene Panel taken?

The Ehlers Danlos Syndrome (EDS) Gene Panel test is taken to diagnose or confirm the presence of Ehlers Danlos Syndrome, a group of genetic connective tissue disorders that affects the skin, joints, and blood vessels. This test analyzes a panel of genes associated with EDS to identify any mutations or variations that may be causing the symptoms of the syndrome.

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