Multiple syndromes of 3-methylglutaconic aciduria

K. Michael Gibson, Orly N. Elpeleg, Cornelius Jakobs, Hanan Costeff, Richard I. Kelley

Research output: Contribution to journalArticle

Abstract

The most common clinical syndromes associated with 3-methylglutaconic aciduria are presented. In some patients these syndromes are multisystemic, progressive disorders of unknown etiology. Tissues deriving significant energy through oxidative metabolism (notably brain and cardiac muscle) are most often affected and in some the primary defect may reside within the mitochondrial respiratory chain. Although increasing biochemical evidence suggests that 3-methylglutaconic aciduria may correlate with deranged mitochondrial energy metabolism, the biochemical origin of 3-methylglutaconic acid and the significance of its increased excretion remain unknown. This review describes these syndromes and illustrates the necessity of urinary organic acid analysis to assist in the differential diagnosis.

Original languageEnglish (US)
Pages (from-to)120-123
Number of pages4
JournalPediatric Neurology
Volume9
Issue number2
DOIs
StatePublished - Jan 1 1993

    Fingerprint

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Neurology
  • Developmental Neuroscience
  • Clinical Neurology

Cite this

Gibson, K. M., Elpeleg, O. N., Jakobs, C., Costeff, H., & Kelley, R. I. (1993). Multiple syndromes of 3-methylglutaconic aciduria. Pediatric Neurology, 9(2), 120-123. https://doi.org/10.1016/0887-8994(93)90046-F