NBS G6PD DEFICIENCY, DRIED BLOOD SPOT
The NBS G6PD deficiency test screens newborns for glucose-6-phosphate dehydrogenase deficiency. This condition can lead to hemolytic anemia, and early diagnosis helps prevent triggers.
NBS G6PD DEFICIENCY, DRIED BLOOD SPOT Test in Mangaluru Overview
No special preparations needed
- Glucose-6-phosphate Dehydrogenase
The neonatal screening G6PD test identifies glucose-6-phosphate dehydrogenase (G6PD) deficiency, a genetic disorder that can cause hemolytic anemia.
It is routinely recommended for newborns in regions with a high prevalence of G6PD deficiency or a family history of the condition.
A heel-prick blood sample is analyzed using enzymatic or molecular methods to assess G6PD activity.
- Low G6PD levels: Suggest G6PD deficiency.
- Normal G6PD levels: Indicate no deficiency.
Test code
3321
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.
Specimen rejection criteria
Test run frequency
Monday,Thursday TIME - 10:30
Turn around time
Next Day
Performing locations
Department
- Eia-neonatal
CPT and Loinc codes
Package price
₹450
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₹450