| Literature DB >> 20861782 |
Marko Culjat1, Vesna Benjak, Andrea Dasovic-Buljevic, David Ozretic, Ksenija Fumic, Cécile Acquaviva, Ivo Baric.
Abstract
We present brain imaging and spectroscopy data in a neonate with a confirmed classic form of nonketotic hyperglycinemia (NKH), an autosomal-recessive metabolic disorder characterized by accumulation of glycine. To our knowledge, this is the first report of such complete analysis of the changes seen on conventional magnetic resonance imaging, diffusion-weighted imaging, and magnetic resonance spectroscopy at such an early age. The findings in a neonate are consistent with reports in older children with NKH, confirming that pathological changes typical for NKH can be seen in the first postnatal week.Entities:
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Year: 2010 PMID: 20861782 DOI: 10.1097/RCT.0b013e3181e846d7
Source DB: PubMed Journal: J Comput Assist Tomogr ISSN: 0363-8715 Impact factor: 1.826