Test Code LAB2969 Cystine, WBC
Additional Codes
Leuk Cyst
Clinical System Name
Cystine, WBC
Synonyms
WBC Intracellular Cystine Assay
Sample Requirements
Specimen: Whole Blood
Container(s): Yellow Top/ACD-Solution A
Preferred Vol: 5.0 - 10.0 mL
Minimum Vol: 2.0 mL
Notes: Test is used for initial diagnosis and for monitoring. This is a time sensitive draw for monitoring: Patients on Cystagon are collected 5-6 hours after their last dose. Patients on Procysbi should have sample collected right before their dose. Note drug, time of last dose on requisition, place whole blood in cold pack and transport to CPA.
Processing Instructions
Reject due to: any tube other than Yellow Top/ACD-Solution A
Spin: N
Aliquot: N
Temp: 2 - 8 C
Storage Location: Place whole blood on cold pack or on ice immediately and transport to CPA. Refrigerate within ONE hour. Note drug (Cystagon or Procysbi) and time of last dose on requisition.
Off-site collection: No off-site collection.
Stability
Specimen Type | Temperature | Time |
---|---|---|
Whole Blood | Refrigerated | 24 hr |
Availability
STAT | Available | TAT |
---|---|---|
N | 21 d |
Performing Laboratory
UCSD Medical Center
Biochemical Genetics Laboratory
CTF Bldg, Room B-213
212 Dickinson Street
San Diego, CA 92103
Phone Number: (619) 543-5260
Department
Department: Send Outs
Phone Number: (206) 987-2563
Methodology
Method:
Analytical Volume: > 2.0 mL Whole Blood
Limitations:
Reference Range
Interpretive report is provided.
Send Out Instructions
Reference Test Name: | WBC Intracellular Cystine Assay |
Reference Test Number: | None specified |
Instructions: | Ship whole blood refrigerated via FedEx Priority Overnight, Monday through Thursday. UCSD's Cystine Determination Laboratory does not accept Saturday delivery. |
Special Instructions
Links to:
UCSD Biochemical Genetics/Cystine Lab
UCSD Biochemical Genetics Requisition Form
Extraction technique:
Clinical Utility
Nephropathic cystinosis in untreated children is characterized by renal tubular Fanconi syndrome, poor growth, hypophosphatemic rickets, impaired glomerular function resulting in complete glomerular failure, and accumulation of cystine crystals in almost all cells, leading to cellular destruction and tissue dysfunction. Cystinosis is inherited in an autosomal recessive manner.