CACNA1D Gene Primary aldosteronism, seizures, and neurologic abnormalities NGS Genetic Test
Short Name: CACNA1D Gene NGS Test
Also known as: CACNA1D Gene Test, Primary Aldosteronism Genetic Test, CACNA1D Mutation Analysis
CACNA1D Gene Primary aldosteronism, seizures, and neurologic abnormalities NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 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 CACNA1D gene that cause primary aldosteronism, seizures, and neurologic abnormalities for accurate diagnosis and management.
- Test Code
- 5492
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 Weeks
- Fasting Required
- No
- Method
- NGS Technology
Sample Collection
Provide clinical history and undergo genetic counseling to draw a family pedigree chart.
Method: Venipuncture or finger prick
Laboratory Analysis
Blood sample will be collected by a trained phlebotomist.
Report Delivery
Apply pressure to the puncture site to prevent bleeding.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify mutations in the CACNA1D gene that cause primary aldosteronism, seizures, and neurologic abnormalities for accurate diagnosis and management.
How to Prepare
- Fast for 8-12 hours if required
- Avoid strenuous activity before sample collection
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is vital for patients with unexplained hypertension and neurological symptoms, helping to identify genetic causes and tailor treatment."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Understanding Your Results
Positive for pathogenic variant
Confirms genetic cause for symptoms; refer for specialist management.
Negative
No mutations detected; consider other diagnostic tests.
If you experience symptoms like high blood pressure, seizures, or developmental delays, consult a doctor for evaluation.
Risks & Considerations
- ●Minimal risk from blood draw
- ●Potential psychological impact of results
Frequently Asked Questions
What is the CACNA1D gene?
What conditions are linked to CACNA1D mutations?
How is primary aldosteronism diagnosed?
What symptoms indicate a need for this test?
What is NGS technology?
What sample is required for the test?
How long does it take to get results?
Is genetic counseling recommended?
What is the cost of the CACNA1D gene test?
Is the test covered by insurance?
Can I get the test done at home?
What should I do if the test is positive?
Related Tests
CYP21A2 Gene Adrenal hyperplasia due to 21-hydroxylase deficiency NGS Genetic Test
₹20,000HSD17B3 Gene Pseudohermaphroditism with gynecomastia NGS Genetic Test
₹20,000CYP27B1 Gene Rickets, vitamin D dependent, type 1 NGS Genetic Test
₹20,000TBCE Gene Hypoparathyroidism-retardation-dysmorphism syndrome NGS Genetic Test
₹20,000TSHR Gene Hypothyroidism congenital nongoitrous type 1 NGS Genetic Test
₹20,000PAX8 Gene Hypothyroidism congenital nongoitrous type 2, familial NGS Genetic Test
₹20,000Reference Laboratory Services
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.
Your Data Privacy
Your medical data is protected under Indian law.
✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
Book Your Test
Enter your details and we'll connect you within 15 minutes.
