A B C D E F G H I J K L M N O P Q R S T U V W X Y Z # |
Adenosine Deaminase, RBC
Test Code39148
Alias/See Also
LAB1373
CPT Codes
82657<br><strong>This test is not available for New York patient testing.</strong>
Preferred Specimen
1 mL whole blood collected in an EDTA (lavender-top or pink-top) or sodium or lithium heparin (green-top) tube
Minimum Volume
1 mL
Transport Temperature
Room temperature
Specimen Stability
Room temperature: 15 days
Refrigerated: 15 days
Frozen: Unacceptable
Refrigerated: 15 days
Frozen: Unacceptable
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Hemolysis
Methodology
Kinetic Spectrophotometry
FDA Status
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
Setup Schedule
Set up: Sun, Tues, Thurs; Report available: 2-5 days
Reference Range
400-900 mU/g Hb
Clinical Significance
Adenosine Deaminase (ADA) deficiency is an autosomal recessive disorder of purine metabolism primarily affecting lymphocyte development, viability, and function. Affected individuals have less than 1 percent of normal ADA catalytic activity in red cell hemolysates. ADA deficiency is the cause of 20-30 percent of SCID cases. If the patient has been recently transfused, ADA deficiency may be masked; interpret results with caution. Heterozygotes cannot be identified by this test.
Performing Laboratory
ARUP
500 Chipeta Way
Salt Lake City, UT 84108