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Creatine Deficiency Syndromes: Diagnostic Pearls and Pitfalls

Published online by Cambridge University Press:  18 February 2016

Claire Hinnell*
Affiliation:
Department of Neurology, King's College Hospital, Ashford, United Kingdom
Michael Samuel
Affiliation:
Department of Neurology, King's College Hospital, Ashford, United Kingdom East Kent Hospitals University NHS Foundation Trust, Ashford, United Kingdom
Fadi Alkufri
Affiliation:
Department of Neurology, King's College Hospital, Ashford, United Kingdom
Keyoumars Ashkan
Affiliation:
Department of Neurosurgery, King's College Hospital, Ashford, United Kingdom
Yusof Rahman
Affiliation:
Guy's and St Thomas' NHS Foundation Trust, London, Ashford, United Kingdom
Charles Turner
Affiliation:
WellChild Laboratory, King's College London, Evelina Children's Hospital, Ashford, United Kingdom Guy's and St Thomas' NHS Foundation Trust, London, Ashford, United Kingdom
R. Neil Dalton
Affiliation:
WellChild Laboratory, King's College London, Evelina Children's Hospital, Ashford, United Kingdom
Lina Nashef
Affiliation:
Department of Neurology, King's College Hospital, Ashford, United Kingdom
*
Foothills Medical Centre, 12th Floor, Neurosciences, 1403 - 29th St. NW, Calgary, Alberta, T2N 2T9, Canada
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Abstract

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Type
Brief Communications
Copyright
Copyright © Canadian Neurological Sciences Federation 2011

References

1.Nasrallah, F, Feki, M, Kaabachi, N. Creatine and creatine deficiency syndromes: biochemical and clinical aspects. Pediatr Neurol. 2010 Mar;42(3):163–71.CrossRefGoogle ScholarPubMed
2.Mercimek-Mahmutoglu, S, Stöckler-Ipsiroglu, S. Gene Reviews: Creatine Deficiency Syndromes. Gene Reviews 2009 February 2010 [cited July 2010]; Available from: http://www.ncbi.nlm. nih.gov/bookshelf/br.fcgi?book=gene&part=creatineGoogle Scholar
3.Mercimek-Mahmutoglu, S, Stoeckler-Ipsiroglu, S, Adami, A, et al.GAMT deficiency: features, treatment, and outcome in an inborn error of creatine synthesis. Neurology. 2006 Aug 8;67(3):480–4.CrossRefGoogle Scholar
4.O’Rourke, DJ, Ryan, S, Salomons, G, Jakobs, C, Monavari, A, King, MD. Guanidinoacetate methyltransferase (GAMT) deficiency: late onset of movement disorder and preserved expressive language. Dev Med Child Neurol. 2009 May;51(5):404–7.CrossRefGoogle ScholarPubMed
5.Verhoeven, NM, Guerand, WS, Struys, EA, Bouman, AA, van der Knaap, MS, Jakobs, C. Plasma creatinine assessment in creatine deficiency: A diagnostic pitfall. J Inherit Metab Dis. 2000 Dec;23(8):835–40.CrossRefGoogle ScholarPubMed