Alpha-Galactosidase Enzyme Activity, Leukocytes




Test Mnemonic

AGALAC

CPT Codes

  • 82657 - QTY (1)

Aliases

  • Fabry Disease Enzyme Test

Includes

  • Alpha-Galactosidase, Leukocytes
  • Interpretation
  • Reviewed By

Performing Laboratory

Mayo Clinic Dpt of Lab Med & Pathology


Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
6 mLWhole bloodACD B (Yellow) RefrigeratedCollect Monday - Wednesday only. Do not collect specimen on the day before a major holiday. Specimen must be sent to Cleveland Clinic Laboratories on the same day as collection. Send specimen in original tube. Do not transfer to other containers.

Alternate Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
6 mLWhole bloodACD A (Yellow) RefrigeratedCollect Monday - Thursday only. Do not collect specimen on the day before a major holiday. Send specimen in original tube. Do not transfer to other containers.
6 mLWhole bloodEDTA (Lavender) RefrigeratedCollect Monday - Thursday only. Do not collect specimen on the day before a major holiday. Send specimen in original tube. Do not transfer to other containers.

Minimum Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
2 mL     

Stability

Environmental Condition Description
Refrigerated6 days (preferred)
Ambient6 days
FrozenUnacceptable

Days Performed

Mon, Wed

Turnaround Time

6 - 10 days

Methodology

Name Description
Flow Injection Analysis-Tandem Mass Spectrometry (FIA-MS/MS) 

Reference Range

Alpha Galactosidase, Leukocytes
Sex Age From Age To Type Range Range Unit
   Years99 YearsNormal>= 10.32nmol/hr/mg protein

Special Info

For optimal isolation of leukocytes, it is recommended that the specimen arrive refrigerated at the performing laboratory within 96 hours of collection to be stabilized. Specimens received after 96 hours could have falsely normal results. Do not collect the day before a major holiday. Specimen should be collected and packaged as close to shipping time as possible. Grossly hemolyzed specimens will be rejected.

Clinical Info

Useful for diagnosing Fabry disease in male patients. Verifying abnormal serum alpha-galactosidase results in male patients with a clinical presentation suggestive of Fabry disease. Results from this assay do not reflect carrier status because of individual variation of alpha-galactosidase enzyme levels. Individuals with pseudodeficiency allelic variants can show reduced alpha-galactosidase A enzyme activity with this assay. Carrier detection using enzyme levels is unreliable in females, and mutation analysis using molecular methods is recommended. Values below the reference range are consistent with a diagnosis Fabry Disease. When abnormal results are detected, a detailed interpretation is given