NBS Biotidinase, Dried Blood Spot
Overview of NBS Biotidinase, Dried Blood Spot in Thrissur
What is the NBS biotinidase test?
This newborn screening (NBS) test detects biotinidase deficiency, a genetic disorder affecting biotin metabolism.
Who should take this test?
All newborns should undergo this test as part of routine metabolic screening.
How is the test performed?
A heel-prick blood sample is analyzed for biotinidase enzyme activity.
What do abnormal results indicate?
Low enzyme levels suggest biotinidase deficiency, which can lead to neurological and skin problems if untreated.
Can biotinidase deficiency be treated?
Yes, through lifelong biotin supplementation.
Test included
- Biotinidase Deficiency
Doctor information
Test code
3320
CPT and Loinc codes
Department
- Eia-neonatal
Turn around time
Next Day
Test run frequency
Monday,Thursday TIME - 10:30
Performing locations
2 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
₹735
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₹735