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CACNA1A Gene Familial Hemiplegic Migraine Type 1 Genetic Test

Original price was: $700.Current price is: $500.

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The CACNA1A Gene Familial Hemiplegic Migraine Type 1 NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the CACNA1A gene responsible for familial hemiplegic migraine type 1. This comprehensive neurological genetic test utilizes Next Generation Sequencing technology to detect specific genetic variations that cause severe migraine episodes accompanied by temporary paralysis. The test provides crucial information for individuals experiencing recurrent hemiplegic migraines, helping to confirm diagnosis, guide treatment strategies, and assess inheritance risks. At only $500 USD, this advanced genetic analysis offers valuable insights for patients and families affected by this rare neurological condition. Results are typically available within 3-4 weeks from blood or DNA samples.

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CACNA1A Gene Familial Hemiplegic Migraine Type 1 NGS Genetic DNA Test

Understanding Familial Hemiplegic Migraine Type 1

Familial Hemiplegic Migraine Type 1 (FHM1) represents a rare and severe form of migraine disorder characterized by temporary paralysis or weakness on one side of the body during migraine attacks. This neurological condition is inherited in an autosomal dominant pattern, meaning a single copy of the mutated gene from either parent can cause the disorder. The CACNA1A gene test provides definitive genetic confirmation for individuals and families affected by this debilitating condition.

What Does the CACNA1A Gene Test Measure?

This advanced genetic test specifically analyzes the CACNA1A gene located on chromosome 19, which encodes the alpha-1A subunit of voltage-gated calcium channels in the brain. These calcium channels play a crucial role in neurotransmitter release and neuronal communication. The test detects:

  • Pathogenic mutations in the CACNA1A gene associated with FHM1
  • Specific nucleotide changes affecting calcium channel function
  • Genetic variations that disrupt normal neuronal signaling
  • Inheritance patterns within affected families

Who Should Consider This Genetic Test?

This specialized neurological genetic test is recommended for individuals experiencing:

  • Recurrent migraine attacks with temporary hemiplegia (one-sided weakness)
  • Family history of hemiplegic migraines or similar neurological symptoms
  • Severe migraine episodes accompanied by aura symptoms lasting hours to days
  • Additional neurological features such as ataxia, seizures, or consciousness alterations
  • Uncertain diagnosis despite comprehensive neurological evaluation
  • Planning for family and reproductive decisions

Clinical Benefits of CACNA1A Genetic Testing

Undergoing this comprehensive genetic analysis provides numerous clinical advantages:

  • Definitive Diagnosis: Confirms or rules out FHM1 with high accuracy
  • Personalized Treatment: Guides appropriate migraine management strategies
  • Family Planning: Provides crucial information for genetic counseling and reproductive decisions
  • Risk Assessment: Identifies at-risk family members for early intervention
  • Prognostic Information: Helps understand potential disease progression and complications
  • Therapeutic Guidance: Informs medication choices and preventive measures

Understanding Your Test Results

Your genetic test results will be carefully interpreted by our expert genetic counselors and neurologists:

  • Positive Result: Indicates a pathogenic mutation in the CACNA1A gene, confirming FHM1 diagnosis
  • Negative Result: Suggests absence of known FHM1-causing mutations in the CACNA1A gene
  • Variant of Uncertain Significance: Identifies genetic changes with unknown clinical impact requiring further evaluation
  • Comprehensive Report: Includes detailed interpretation, clinical implications, and family counseling recommendations

Test Specifications and Pricing

Test Component Details
Test Name CACNA1A Gene Familial Hemiplegic Migraine Type 1 NGS Genetic DNA Test
Regular Price $700 USD
Discount Price $500 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card
Testing Method Next Generation Sequencing (NGS) Technology

Pre-Test Requirements

Before scheduling your CACNA1A genetic test, we recommend:

  • Complete clinical history documentation of neurological symptoms
  • Genetic counseling session to create detailed family pedigree chart
  • Discussion of test implications, benefits, and limitations
  • Informed consent process understanding potential outcomes

Nationwide Testing Availability

We provide comprehensive genetic testing services across the United States with convenient locations in major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, and Philadelphia. Our state-of-the-art laboratories ensure accurate and reliable results for patients nationwide.

Take Control of Your Neurological Health

Don’t let uncertainty about your migraine condition affect your quality of life. The CACNA1A Gene Familial Hemiplegic Migraine Type 1 NGS Genetic DNA Test provides the clarity needed for proper diagnosis and management. Our team of genetic specialists and neurologists are ready to support you through every step of the testing process.

Ready to schedule your genetic test? Contact our genetic counseling team today at +1(267) 388-9828 or book your appointment online. Take the first step toward understanding your neurological health and making informed decisions about your care.