Analyzer 26 SMA 26 Test Panel Test
Short Name: SMA 26 Test Panel
Also known as: SMA Carrier Test, Analyzer 26 Panel, Genetic Disorder Screening
Analyzer 26 SMA 26 Test Panel Test test available at DNA Labs India for ₹3,000. Uses Spectrophotometry, Indirect ISE, Hexokinase, PCR for Genetic Analysis on Serum and Plasma samples. Results in Results are typically available within 3-5 days after sample collection.. 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
The purpose of the Analyzer 26 SMA 26 Test Panel is to diagnose spinal muscular atrophy by assessing mutations in the SMN1 and SMN2 genes, while also evaluating key biochemical parameters for a holistic health check. This includes measuring glucose (fasting and postprandial), urea, creatinine, uric acid, cholesterol, triglycerides, CPK, HBDH, LDH, AST (SGOT), ALT (SGPT), GGTP, bilirubin (total, direct, indirect), total protein, albumin, A:G ratio, alkaline phosphatase, calcium, phosphorus, sodium, potassium, chloride, and amylase. These parameters help in detecting SMA and monitoring associated metabolic or organ functions, providing a comprehensive diagnostic and screening tool for individuals at risk or with symptoms of genetic disorders.
- Test Code
- 116
- Price
- ₹3,000
- Sample Type
- Serum and Plasma
- Result Time
- Results are typically available within 3-5 days after sample collection.
- Fasting Required
- Yes (12 hours)
- Method
- Spectrophotometry, Indirect ISE, Hexokinase, PCR for Genetic Analysis
Sample Collection
Ensure 12 hours overnight fasting before sample collection. Avoid heavy meals or strenuous activity prior to the test.
Method: Venipuncture
Laboratory Analysis
A healthcare professional will collect blood samples via venipuncture into specified tubes (SST for serum, Grey Top for plasma).
Report Delivery
Apply pressure to the puncture site to prevent bleeding. Resume normal activities unless advised otherwise. Keep the collected samples refrigerated or frozen as instructed.
Timeline: Results are typically available within 3-5 days after sample collection.
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the Analyzer 26 SMA 26 Test Panel is to diagnose spinal muscular atrophy by assessing mutations in the SMN1 and SMN2 genes, while also evaluating key biochemical parameters for a holistic health check. This includes measuring glucose (fasting and postprandial), urea, creatinine, uric acid, cholesterol, triglycerides, CPK, HBDH, LDH, AST (SGOT), ALT (SGPT), GGTP, bilirubin (total, direct, indirect), total protein, albumin, A:G ratio, alkaline phosphatase, calcium, phosphorus, sodium, potassium, chloride, and amylase. These parameters help in detecting SMA and monitoring associated metabolic or organ functions, providing a comprehensive diagnostic and screening tool for individuals at risk or with symptoms of genetic disorders.
How to Prepare
- Fast for 12 hours overnight before sample collection.
- Use the specified tubes: SST tube for serum and Grey Top (Sodium Fluoride) tube for plasma.
- Collect samples as per instructions: 3 mL serum and 2 mL plasma.
- Ship samples refrigerated or frozen to maintain stability.
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Early diagnosis of spinal muscular atrophy through genetic testing like this panel is essential for timely intervention, management, and family planning. Genetic counseling is recommended for affected families."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted samples
- Insufficient sample volume
- Use of incorrect collection tubes
- Samples not stored or shipped as required
Understanding Your Results
No evidence of SMA carrier status; normal risk.
Carrier of SMA; may pass the mutation to offspring. Genetic counseling advised.
Diagnosis of spinal muscular atrophy; clinical correlation and specialist consultation recommended.
May indicate metabolic issues, organ dysfunction, or secondary effects of SMA; further evaluation needed.
No significant metabolic abnormalities detected; continue monitoring if symptoms persist.
Consult a doctor immediately if you experience muscle weakness, difficulty breathing, or if the test results indicate SMA or abnormal parameters. Genetic counseling is recommended for family planning if carrier status is identified.
Limitations
- ⚠May not detect all rare SMN1 or SMN2 mutations
- ⚠Results should be confirmed with clinical evaluation and other tests
- ⚠Biochemical parameters may vary with diet, hydration, or other conditions
- ⚠Genetic counseling is recommended for interpretation of genetic results
Risks & Considerations
- ●Minor bruising or pain at the blood draw site
- ●Rare risk of infection or dizziness
- ●Psychological impact of genetic results
Interfering Factors
- ●Hemolyzed or lipemic samples
- ●Improper fasting or sample handling
- ●Recent medications affecting biochemical parameters
- ●Incorrect sample collection or storage
Compare With Similar Tests
| Test | Analyzer 26 SMA 26 Test Panel | SMN1 Gene Deletion Test | Creatine Kinase Test | Full Genetic Panel | Basic Metabolic Panel |
|---|---|---|---|---|---|
| Comparison | Analyzer 26 SMA 26 Test Panel |
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