CACNA1A Gene Familial hemiplegic migraine type 1 NGS Genetic Test
Short Name: CACNA1A Gene FHM1 NGS Test
Also known as: Familial Hemiplegic Migraine Type 1 Genetic Test, CACNA1A Mutation Analysis
CACNA1A Gene Familial hemiplegic migraine type 1 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA samples. Results in 3-4 weeks. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
To identify mutations in the CACNA1A gene for diagnosis of Familial Hemiplegic Migraine Type 1.
- Test Code
- 1615
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA
- Result Time
- 3-4 weeks
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
No specific preparation required, but genetic counseling recommended.
Method: Venipuncture or FTA card collection
Laboratory Analysis
Blood sample collected via venipuncture or on FTA card.
Report Delivery
Apply pressure to puncture site; store sample properly.
Timeline: 3-4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify mutations in the CACNA1A gene for diagnosis of Familial Hemiplegic Migraine Type 1.
How to Prepare
- Use sterile equipment
- Label samples correctly
- Follow home collection guidelines if applicable
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing for CACNA1A mutations is crucial for diagnosing familial hemiplegic migraine, especially in families with a history of neurological disorders."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted samples
- Insufficient volume
- Unlabeled samples
Understanding Your Results
Positive for pathogenic variant
Confirms diagnosis of FHM1; genetic counseling advised.
Negative
No mutation detected; clinical correlation recommended.
Variant of uncertain significance
Further testing or family studies may be needed.
If symptoms of hemiplegic migraine occur, or for family members of affected individuals.
Limitations
- ⚠May not detect all types of mutations (e.g., large deletions)
- ⚠Results require genetic counseling for interpretation
Risks & Considerations
- ●Bruising
- ●Infection (rare)
- ●Fainting
Interfering Factors
- ●DNA degradation
- ●Sample contamination
- ●Hemolyzed blood sample
Compare With Similar Tests
| Test | CACNA1A Gene Familial hemiplegic migraine type 1 NGS Genetic Test | ||||
|---|---|---|---|---|---|
| Comparison | CACNA1A Gene Familial hemiplegic migraine type 1 NGS Genetic Test |
Frequently Asked Questions
What is the CACNA1A Gene Test?
Why is this test recommended for Familial Hemiplegic Migraine?
How is the test performed?
What are the symptoms of Familial Hemiplegic Migraine Type 1?
How long does it take to get the test results?
Is home sample collection available for this test?
What is the cost of the CACNA1A Gene Test?
Can this test be used for prenatal diagnosis?
What does a positive test result mean?
What are the limitations of the test?
Is genetic counseling required before taking the test?
How accurate is the NGS genetic test for CACNA1A?
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We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
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