6310 : Acylglycines, Quant. Urine
INFORMATION:
Alternate Name:
Acylglycines, Quant.
Methodology:
Gas Chromat. Mass Spectrometry
Clinical Utility:
Diagnosis and monitoring for patients affected with 1 of the following inborn errors of metabolism. Fatty Acid Oxidation Disorders: Glutaric acidemia type II; Medium-chain 3-ketoacyl-CoA thiolase (MCKAT) deficiency; Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency; Short chain acyl-CoA dehydrogenase (SCAD) deficiency. Organic Acidurias: 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (2M3HBD) deficiency; -2-Methylbutyryl-CoA dehydrogenase deficiency; -3-Methylcrotonyl-CoA carboxylase deficiency; -3-Methylglutaconyl-CoA-hydratase deficiency; -Aminoacylase 1 deficiency; -Beta-ketothiolase deficiency; -Ethylmalonic encephalopathy; -Glutaryl-CoA dehydrogenase deficiency; -Isobutyryl-CoA dehydrogenase (IBD) deficiency; -Isovaleryl-CoA dehydrogenase deficiency; -Multiple carboxylase deficiency; -Propionic acidemia.
ORDERING:
Test Code:
6310-7
Turnaround Time:
16 DAYS
Preferred Specimen:
13 mL Urine Cup
Collection:
Container | Qty | Temp | Stability |
---|---|---|---|
Urine Cup | 1 | Refrigerate | 9 DAYS |
Collection Instructions:
USC: Collect urine in cup, label with patients name
Storage Transport Instructions:
Refrig.
Alternative Specimen:
Urine Container - 24hr, Urine tube without preservative, Urine Cup 24 hour
Billing:
CPT Codes:
82542 x 1
CPT Code Disclaimer
CPT codes provided are for informational purposes only. Accuracy of CPT presented should be validated prior to consideration for billing.
CPT coding is the sole responsibility of the billing party. Please direct any questions regarding CPT coding to the payer being billed.