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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 report for the Familial Hemiplegic Migraine Gene Panel test can be obtained within a maximum of 21 days.

What are the prerequisites for the test Familial Hemiplegic Migraine Gene Panel

  • Completed Test Requisition Form
  • 5-10 mL whole blood in a lavender top (EDTA) tube
  • Minimum volume of 2 mL whole blood in a lavender top (EDTA) tube for patients under 2 years of age
  • Patient's insurance information
  • Completed patient consent form

What are the measure values for the test Familial Hemiplegic Migraine Gene Panel

  • ATP1A2 Gene Analysis: Mutations Detected or Not Detected
  • ATP1A2 Gene Deletion/Duplication Analysis: Deletion/Duplication Detected or Not Detected
  • CACNA1A Gene Analysis: Mutations Detected or Not Detected
  • CACNA1A Gene Deletion/Duplication Analysis: Deletion/Duplication Detected or Not Detected
  • SCN1A Gene Analysis: Mutations Detected or Not Detected
  • SCN1A Gene Deletion/Duplication Analysis: Deletion/Duplication Detected or Not Detected

What does this test Familial Hemiplegic Migraine Gene Panel identify?

Familial Hemiplegic Migraine Gene Panel

The Familial Hemiplegic Migraine Gene Panel is a genetic test that identifies mutations in specific genes associated with familial hemiplegic migraine (FHM). FHM is a rare form of migraine that is characterized by temporary paralysis or weakness on one side of the body, along with other migraine symptoms.

The gene panel typically includes analysis of genes such as CACNA1A, ATP1A2, and SCN1A, which are known to be linked to FHM. Mutations in these genes can disrupt the normal functioning of ion channels in the brain, leading to abnormal electrical activity and triggering migraine attacks.

By analyzing the DNA of an individual for mutations in these specific genes, the Familial Hemiplegic Migraine Gene Panel can help confirm a diagnosis of FHM and provide valuable information for personalized treatment and management strategies.

Why is this test Familial Hemiplegic Migraine Gene Panel taken?

Familial Hemiplegic Migraine Gene Panel Test

The Familial Hemiplegic Migraine Gene Panel Test is taken to identify mutations in specific genes associated with Familial Hemiplegic Migraine (FHM). FHM is a rare form of migraine that is inherited in families and is characterized by severe, debilitating headaches accompanied by temporary paralysis or weakness on one side of the body.

By analyzing the genes known to be involved in FHM, this test can help diagnose individuals with a family history of the condition or suspected FHM symptoms. It can also provide information on the specific genetic mutations present, which can aid in treatment decisions and genetic counseling.

Overall, the Familial Hemiplegic Migraine Gene Panel Test is crucial for identifying the underlying genetic cause of FHM and guiding personalized care for individuals affected by this condition.

Popular FAQs on Test

The Familial Hemiplegic Migraine Gene Panel test is a genetic test that analyzes specific genes known to be associated with familial hemiplegic migraine, a rare form of migraine that runs in families.
Individuals with a family history of hemiplegic migraine or individuals who have been diagnosed with hemiplegic migraine may consider getting the test to understand their genetic risk factors.
The test is typically done using a blood or saliva sample, which is then analyzed in a laboratory to identify any mutations or variations in the specific genes associated with familial hemiplegic migraine.
The test can provide valuable information about an individual's genetic risk for hemiplegic migraine, which can help with diagnosis, treatment, and family planning decisions.
Coverage for the test may vary depending on the individual's insurance plan. It is recommended to check with the insurance provider to determine coverage and any out-of-pocket costs.

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