| Literature DB >> 17641269 |
J Vodopiutz1, C B Item, M Häusler, H Korall, O A Bodamer.
Abstract
Guanidinoacetate methyltransferase deficiency typically presents with muscular hypotonia, global developmental delay, extrapyramidal signs, and seizures during infancy and childhood. The authors report a 5-year-old child with guanidinoacetate methyltransferase deficiency who presented with severe speech delay, emphasizing the importance of an early screening for disorders of creatine synthesis and transport in every infant or child with isolated speech delay of unknown cause.Entities:
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Year: 2007 PMID: 17641269 DOI: 10.1177/0883073807304015
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987