Clinical characteristics and diagnostic clues in inborn errors of creatine metabolism

C. Stromberger, O. A. Bodamer, S. Stöckler-Ipsiroglu

Research output: Contribution to journalArticlepeer-review

109 Scopus citations

Abstract

Creatine deficiency syndromes are a newly described group of inborn errors of creatine synthesis (arginine:glycine amidinotransferase (AGAT) deficiency and guanidinoaceteate methyltransferase (GAMT) deficiency) and creatine transport (creatine transporter (CRTR) deficiency). The common clinical denominator of creatine deficiency syndromes is mental retardation and epilepsy, suggesting the main involvement of cerebral grey matter (grey matter disease). Patients with GAMT deficiency exhibit a more complex clinical phenotype with dystonic hyperkinetic movement disorder and epilepsy that in some cases is unresponsive to pharmacological treatment. The common biochemical denominator of creatine deficiency syndromes is cerebral creatine deficiency which is demonstrated by in vivo proton magnetic resonance spectroscopy. Measurement of guanidinoacetate in body fluids may discriminate GAMT (high concentration), AGAT (low concentration) and CRTR (normal concentration). Further biochemical characteristics include changes in creatine and creatinine concentrations in body fluids. GAMT and AGAT deficiency are treatable by oral creatine supplementation, while patients with CRTR deficiency do not respond to this type of treatment. Further recognition of patients will be of major importance for the estimation of the frequency, for the understanding of phenotypic variations and for treatment strategies.

Original languageEnglish (US)
Pages (from-to)299-308
Number of pages10
JournalJournal of Inherited Metabolic Disease
Volume26
Issue number2-3
DOIs
StatePublished - Jan 1 2003

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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