Test Code LALB Lysosomal Acid Lipase, Blood
Useful For
Evaluation of patients with a clinical presentation suggestive of lysosomal acid lipase deficiency using blood specimens
This test is not useful to determine carrier status for cholesteryl ester storage disease or Wolman disease.
Special Instructions
Reporting Name
Lysosomal Acid Lipase, BSpecimen Type
Whole bloodSpecimen Required
Container/Tube:
Preferred: Lavender top (EDTA)
Acceptable: Yellow top (ACD) or green top (sodium heparin)
Specimen Volume: 2 mL
Specimen Minimum Volume
0.5 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Whole blood | Refrigerated (preferred) | 7 days | |
Ambient | 7 days |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Reference Values
≥21.0 nmol/h/mL
Day(s) Performed
Friday
Report Available
8 to 15 daysSpecimen Retention Time
1 yearPerforming Laboratory
Mayo Clinic Laboratories in RochesterCPT Code Information
82657
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
LALB | Lysosomal Acid Lipase, B | 73958-1 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
62954 | Lysosomal Acid Lipase, B | 73958-1 |
36339 | Reviewed By | 18771-6 |
36338 | Interpretation (LALB) | 59462-2 |
Forms
1. New York Clients-Informed consent is required. Document on the request form or electronic order that a copy is on file. The following documents are available:
-Informed Consent for Genetic Testing (T576)
-Informed Consent for Genetic Testing-Spanish (T826)
2. Biochemical Genetics Patient Information (T602)
3. If not ordering electronically, complete, print, and send 1 of the following forms with the specimen:
Genetics Test Information
This test provides diagnostic testing for patients with clinical signs and symptoms suspicious for lysosomal acid lipase deficiency (LALD).
LALD is expressed phenotypically as infantile-onset Wolman disease or later-onset cholesterol ester storage disease.