Amino Acid, Urine

BC6010U

Synonym(s):
Specimen Container
Wide mouth sterile container
Specimen Requirement
Urine
3 mL
Specimen Storage/Transport
Fresh urine and no preservative. Please send with a separate ice pack.
Orderable as Urgent? For URGENT analysis, contact the Biochemical Genetics lab on 6394 8728 or the Lead Scientist on 8388 8741 to discuss.
Turn Around Time
5 working days
Reference Value(s)
 

Urine amino acid reference ranges in µmol/mmol creatinine

AnalyteAge
0-1m1-6m6m-2yr2-10yr10-13yr>13yr
TAURINE8-2266-899-15913-23018-17616-160
ASPARTATE2-122-163-121-91-92-7
THREONINE20-13817-9214-629-488-287-29
SERINE50-28242-19445-13723-9423-6721-50
ASPARAGINE0-840-580-360-300-180-23
GLUTAMINE0-300-290-180-100-90-12
GLUTAMINE52-20563-22962-19731-23620-11220-76
PROLINE9-2130-1300-140-90-90-9
GLYCINE165-1097210-743110-44584-36264-16543-173
ALANINE62-24462-20636-16217-11521-6216-68
CITRULLINE0-110-100-80-60-50-4
VALINE3-264-196-213-203-173-13
METHIONINE7-276-227-293-213-102-16
CYSTINE23-7813-4810-298-307-236-34
ISOLEUCINE0-60-50-60-60-60-4
LEUCINE3-254-123-173-183-142-11
TYROSINE6-5512-5211-547-356-252-23
PHENYLALANINE4-327-2810-315-265-172-19
BETA AMINOISOBUTYRIC ACID0-870-2160-2660-1750-580-91
ORNITHINE0-190-130-80-70-60-5
LYSINE22-17115-19913-7910-6810-567-58
HISTIDINE80-29592-27887-28745-25543-15926-153
3-METHYLHISTIDINE20-3919-4020-5718-6120-5619-47
ARGININE0-140-110-110-90-60-5
Testing Laboratory Location KKH
Laboratory Biochemical Genetics Lab
Contact Number 6394 8728
Day and Time Performed
Mon – Fri: 0900 hrs – 1800 hrs
Orderable on CPOE? Yes
Downtime Form

Biochemical Genetics Lab

Additional Information
​​Useful For
  • ​Detecting disorders such as phenylketonuria(PKU), tyrosinaemia, maple syrup urine disease(MSUD), cystinuria, homocystinuria and the urea cycle disorders.
  • Monitoring the efficacy of treatment in patients with these disorders, as well as patients on low protein diets for other reasons (eg. those with organic acidaemias).
​Clinical Indication
  • ​acute life-threatening episode
  • failure to thrive
  • recurrent vomiting
  • neurological deterioration
  • hyperammonaemia
  • lethargy
  • metabolic acidosis
  • testing or following therapy for a specific inborn error of metabolism (PKU, MSUD, tyrosinemia, etc.).
​Interpretation​A detailed interpretation requires the overview of results and correlation to available clinical information. Further steps such as additional biochemical and in vitro studies (enzyme & molecular analysis) may be needed to confirm and provide differential diagnosis of the disorders.
   
For URGENT analysis, contact the Biochemical Genetics laboratory at 6394 8728 or the Lead Scientist at 8388 8741 to discuss.
 
If sent after office hours, urine will be stored in Clinical Laboratory -20°C freezer.

Change History Notes

  • 02 Jul 2025 03:00 PM

    Update day/time performed.

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Last Updated - 02 Jul 2025