Literature DB >> 10762171

Mental retardation and behavioral problems as presenting signs of a creatine synthesis defect.

M S van der Knaap1, N M Verhoeven, P Maaswinkel-Mooij, P J Pouwels, W Onkenhout, E A Peeters, S Stöckler-Ipsiroglu, C Jakobs.   

Abstract

Recently, 3 patients with a creatine synthesis defect have been described. They presented with developmental regression, extrapyramidal movement abnormalities, and intractable epilepsy, and they improved with treatment of creatine monohydrate. We report 2 unrelated boys with a creatine synthesis defect and nonspecific presenting signs of psychomotor retardation, behavioral problems, and, in 1, mild epilepsy. Metabolic urine screening revealed elevations in all metabolites, expressed as millimoles per mole of creatinine, which suggests decreased creatinine excretion. This finding led to the correct diagnosis. We propose to include the assessment of the overall concentrations of amino acids and organic acids relative to creatinine in routine metabolic urine screening.

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Year:  2000        PMID: 10762171     DOI: 10.1002/1531-8249(200004)47:4<540::aid-ana23>3.3.co;2-b

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  21 in total

1.  X-linked creatine-transporter gene (SLC6A8) defect: a new creatine-deficiency syndrome.

Authors:  G S Salomons; S J van Dooren; N M Verhoeven; K M Cecil; W S Ball; T J Degrauw; C Jakobs
Journal:  Am J Hum Genet       Date:  2001-04-20       Impact factor: 11.025

Review 2.  Inborn errors of metabolism for the diagnostic radiologist.

Authors:  Chris J Hendriksz
Journal:  Pediatr Radiol       Date:  2008-12-13

Review 3.  Creatine and its potential therapeutic value for targeting cellular energy impairment in neurodegenerative diseases.

Authors:  Peter J Adhihetty; M Flint Beal
Journal:  Neuromolecular Med       Date:  2008-11-13       Impact factor: 3.843

4.  Characterization of AGAT, GAMT and CT1 in amphioxus: implications for the evolutionary conservation of creatine metabolism related molecules at the invertebrate-to-vertebrate transition.

Authors:  Lifeng Wang; Dongyan Chen; Ying Zhang; Yushuang Lin; Jianwei Li; Hongwei Zhang
Journal:  Dev Genes Evol       Date:  2008-09-05       Impact factor: 0.900

5.  Gatm, a creatine synthesis enzyme, is imprinted in mouse placenta.

Authors:  Lisa L Sandell; Xiao-Juan Guan; Robert Ingram; Shirley M Tilghman
Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-01       Impact factor: 11.205

6.  Arginine:glycine amidinotransferase deficiency: the third inborn error of creatine metabolism in humans.

Authors:  C B Item; S Stöckler-Ipsiroglu; C Stromberger; A Mühl; M G Alessandrì; M C Bianchi; M Tosetti; F Fornai; G Cioni
Journal:  Am J Hum Genet       Date:  2001-09-10       Impact factor: 11.025

7.  Glycine N-methyltransferase deficiency: a novel inborn error causing persistent isolated hypermethioninaemia.

Authors:  S H Mudd; R Cerone; M C Schiaffino; A R Fantasia; G Minniti; U Caruso; R Lorini; D Watkins; N Matiaszuk; D S Rosenblatt; B Schwahn; R Rozen; L LeGros; M Kotb; A Capdevila; Z Luka; J D Finkelstein; A Tangerman; S P Stabler; R H Allen; C Wagner
Journal:  J Inherit Metab Dis       Date:  2001-08       Impact factor: 4.982

8.  Creatine transporters: a reappraisal.

Authors:  Oliver Speer; Lukas J Neukomm; Robyn M Murphy; Elsa Zanolla; Uwe Schlattner; Hugues Henry; Rodney J Snow; Theo Wallimann
Journal:  Mol Cell Biochem       Date:  2004 Jan-Feb       Impact factor: 3.396

Review 9.  Clinical characteristics and diagnostic clues in inborn errors of creatine metabolism.

Authors:  C Stromberger; O A Bodamer; S Stöckler-Ipsiroglu
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

Review 10.  X-linked creatine transporter defect: an overview.

Authors:  G S Salomons; S J M van Dooren; N M Verhoeven; D Marsden; C Schwartz; K M Cecil; T J DeGrauw; C Jakobs
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

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