APOA5 Gene Hyperchylomicronemia type 5 NGS Genetic Test
Short Name: APOA5 Hyperchylomicronemia Type 5 Test
Also known as: Familial Chylomicronemia Syndrome
APOA5 Gene Hyperchylomicronemia type 5 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 genetic mutations in the APOA5 gene that cause hyperchylomicronemia type 5, aiding in diagnosis, management, and genetic counseling.
- Test Code
- 2085
- 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
Genetic counseling session recommended to understand the test and implications.
Method: Venipuncture or FTA Card
Laboratory Analysis
Blood sample collected via venipuncture or using FTA card.
Report Delivery
Sample sent to laboratory for NGS analysis.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify genetic mutations in the APOA5 gene that cause hyperchylomicronemia type 5, aiding in diagnosis, management, and genetic counseling.
How to Prepare
- Ensure proper sample labeling
- Avoid hemolyzed samples
- Follow aseptic techniques
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing for hyperchylomicronemia type 5 is crucial for early diagnosis and management to prevent complications like pancreatitis. Referral for genetic counseling and family screening is recommended."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Sample incorrectly labeled
- Insufficient sample volume
- Contaminated sample
Understanding Your Results
Confirms diagnosis of hyperchylomicronemia type 5; management and genetic counseling recommended.
Does not rule out other causes; clinical correlation advised.
If symptoms of hyperchylomicronemia type 5 are present or if there is a family history of the disorder, consult a geneticist or lipidologist.
Limitations
- ⚠Test may not detect all mutations in the APOA5 gene
- ⚠Results require genetic counseling for interpretation
- ⚠Not a standalone diagnostic; clinical correlation needed
Risks & Considerations
- ●Minimal risk from blood draw
- ●Psychological impact of genetic diagnosis
Interfering Factors
- ●Degraded DNA sample
- ●Contaminated sample
- ●Incorrect sample type
Frequently Asked Questions
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