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DBS Biotidinase, > 1 Mth

This test screens for biotinidase deficiency in infants older than one month using dried blood spot samples. It helps detect potential metabolic disorders that affect hair, skin, and neurological functions.

Also known asNBS -DBS Biotidinase> 1 Month NBS -DBS Biotidinase> 1 Month

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

Next Day

Test details

DBS Biotidinase, > 1 Mth Test in Kharar Overview

Preparations

No special preparations needed

Test included
DBS Biotidinase, > 1 Mth includes 1 parameter

  • Biotinidase Enzyme Activity
Frequently Asked Questions

This test measures biotinidase enzyme activity to diagnose biotinidase deficiency, a rare genetic disorder affecting biotin metabolism.

This test is recommended for:

  • Newborns as part of neonatal screening.
  • Infants with developmental delay, seizures, or skin rashes.
  • Children with unexplained neurological symptoms.

A heel prick or blood sample is analyzed using enzyme assay methods.

  • Normal Biotinidase Activity: No biotinidase deficiency.
  • Partial Deficiency: May require biotin supplementation.
  • Severe Deficiency: Requires immediate biotin therapy.

Early detection and treatment prevent developmental delays, seizures, and other complications.

Test code

9359

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Blood SpotNeoNatal Cards2 SPOTS

Specimen stability information

Blood Spot

Collection instructions

TEST FOR MORE THAN ONE MONTH OLD BABY. 5 DRIED BLOOD SPOTS.CLINICAL HISTORY AND DIET DETAILS REQUIRED

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

DBS Biotidinase, > 1 Mth

₹530

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