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Tiglylglycine
Detects the organic acid tiglylglycine in urine indicating fatty acid metabolism dysfunction.
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
30484-0Primary47954-354342-1Available Lab Tests
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