Tiglylglycine

ChemistryAlso known as: N-TigloylglycineN/A

Detects the organic acid tiglylglycine in urine indicating fatty acid metabolism dysfunction.

Normal Range
Consult your provider
N/A
Abnormal Levels
Consult your provider
Specimen Type
Blood

Why This Biomarker Matters

Presence suggests rare genetic fatty acid oxidation disorders. Early detection enables specialized treatment and energy management strategies.

Overview

Tiglylglycine is a urinary organic acid metabolite that indicates a specific pattern of fatty acid metabolism dysfunction. Its presence in urine suggests possible fatty acid oxidation disorders, particularly short-chain acyl-CoA dehydrogenase (SCAD) deficiency or related metabolic conditions. These rare genetic disorders impair the body's ability to break down certain fats for energy, potentially causing fatigue, muscle weakness, or developmental delays. Detecting tiglylglycine helps identify these serious metabolic disorders requiring specialized management.

Research & Evidence

1 publications

Research data from MEDLINE/PubMed · 1 articles

Technical Information (LOINC Codes)

Standardized laboratory codes for this biomarker

30484-0Primary
Tiglylglycine [Presence] in Urine
47954-3
Tiglylglycine [Moles/volume] in Plasma
umol/L
54342-1
Tiglylglycine [Moles/volume] in Cerebral spinal fluid
umol/L

Available Lab Tests

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