NBS G6PD Deficiency, Dried Blood Spot
Overview of NBS G6PD Deficiency, Dried Blood Spot in Kasaragod
What is the neonatal screening G6PD test?
The neonatal screening G6PD test identifies glucose-6-phosphate dehydrogenase (G6PD) deficiency, a genetic disorder that can cause hemolytic anemia.
When is the neonatal screening G6PD test recommended?
It is routinely recommended for newborns in regions with a high prevalence of G6PD deficiency or a family history of the condition.
How is the test performed?
A heel-prick blood sample is analyzed using enzymatic or molecular methods to assess G6PD activity.
What do the results indicate?
Low G6PD levels: Suggest G6PD deficiency.
Normal G6PD levels: Indicate no deficiency.
Test included
- Glucose-6-phosphate Dehydrogenase
Doctor information
Test code
3321
CPT and Loinc codes
Department
- Eia-neonatal
Turn around time
Next Day
Test run frequency
Monday,Thursday TIME - 10:30
Performing locations
4 labs across India
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Blood Spot | NeoNatal Cards | 1 |
Specimen stability information
Blood Spot
Collection instructions
Complete CLINICAL HISTORY form including birth date & birth time.(Dried Blood spot should be ideally collected within 2nd and 5th day of life after birth).Avoid touching and smearing of the blood spots.The dried blood specimen should be transported or mailed to the laboratory as soon as they are dry (Minimum of 3 Hrs.) and no later than 24 hrs after collection.
Test price
₹450
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₹450