Galactosemia Panel 3 Test
Short Name: Galactosemia Panel 3
Also known as: Galactosemia Genetic Panel, Galactosemia Enzyme Panel
Galactosemia Panel 3 Test test available at DNA Labs India for ₹4,563. Uses Spot Test, Enzyme Assay on Whole blood samples. Results in Report available in 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
To diagnose galactosemia by analyzing genetic mutations in the GALT, GALK1, and GALE genes, aiding in confirmation and management of the disorder.
- Test Code
- 636
- Price
- ₹4,563
- Sample Type
- Whole blood
- Result Time
- Report available in 5 days after sample collection.
- Fasting Required
- No
- Method
- Spot Test, Enzyme Assay
Sample Collection
Avoid sample collection for 60 days post transfusion. Provide clinical and drug history.
Method: Venipuncture
Laboratory Analysis
Blood sample collected via venipuncture from a vein.
Report Delivery
Sample is refrigerated and sent to the laboratory for analysis.
Timeline: Report available in 5 days after sample collection.
Patient Instructions
About This Test
Who Should Get This Test
To diagnose galactosemia by analyzing genetic mutations in the GALT, GALK1, and GALE genes, aiding in confirmation and management of the disorder.
How to Prepare
- Collect 4 mL (2 mL min.) whole blood in 1 Green Top (Sodium Heparin) tube
- Ship refrigerated, do not freeze
- Ensure sample is labeled correctly
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Early diagnosis and galactose-free diet are key to managing galactosemia and preventing long-term complications."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Sample collected within 60 days post transfusion
- Inadequate sample volume or hemolyzed sample
- Missing clinical and drug history
Understanding Your Results
If newborns or infants show symptoms such as jaundice, poor feeding, vomiting, lethargy, or developmental delays.
Limitations
- ⚠May not detect all rare or novel mutations
- ⚠Results require clinical correlation and may need confirmatory testing
Risks & Considerations
- ●Minimal risks from blood draw: bruising, pain, or rare infection at the site
Interfering Factors
- ●Recent blood transfusion within 60 days
- ●Incomplete clinical and drug history
Frequently Asked Questions
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