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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

Maximum Days to Obtain Report for Epileptic Encephalopathy Gene Panel Test

The report for the Epileptic Encephalopathy Gene Panel test can be obtained within 14-21 business days from the date of sample collection.

What are the prerequisites for the test Epileptic Encephalopathy Gene Panel

  • Written informed consent from the patient or legal guardian
  • Clinical information form completed by a healthcare provider
  • 2-5 mL of peripheral blood collected in an EDTA tube
  • Requisition form with patient information and test requested
  • Payment information or insurance authorization

What are the measure values for the test Epileptic Encephalopathy Gene Panel

Gene Measure Value
STXBP1 0.1
SCN1A 0.05
CDKL5 0.08
SLC2A1 0.12

What does this test Epileptic Encephalopathy Gene Panel identify?

  • Epileptic Encephalopathy Gene Panel identifies mutations in genes associated with epileptic encephalopathy.
  • It helps in diagnosing the genetic cause of epileptic encephalopathy in patients.
  • The panel includes genes known to be involved in various types of epileptic encephalopathy, such as Dravet syndrome, Lennox-Gastaut syndrome, and Ohtahara syndrome.
  • Identifying mutations in these genes can help in providing a more accurate diagnosis, prognosis, and personalized treatment plan for patients with epileptic encephalopathy.
  • Overall, the Epileptic Encephalopathy Gene Panel plays a crucial role in genetic testing and management of patients with epileptic encephalopathy.

Why is this test Epileptic Encephalopathy Gene Panel taken?

Test: Epileptic Encephalopathy Gene Panel

Reason for test:

  • This test is taken to diagnose and identify genetic mutations associated with epileptic encephalopathy, a severe form of epilepsy characterized by seizures, developmental delays, and cognitive impairments.
  • Identifying specific genetic mutations can help in providing accurate diagnosis, prognosis, and personalized treatment options for individuals with epileptic encephalopathy.
  • Early detection of genetic mutations can also help in genetic counseling for family members and aid in family planning decisions.

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