Stockport Pathology

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InvestigationBIOTINIDASE ACTIVITY
IndicationsSevere or partial carboxylase deficiency- autosomal recessive condition
Specimen Type2 x Green top
Request FormBlood Sciences or Electronic
Appropriate testing /re-testing interval6m
Related testsNone
HOW TO guidesNone
Information leafletsNone
PublicationsNone
GuidelinesNone