| Literature DB >> 17520433 |
G Sonmez1, H Mutlu, E Ozturk, H O Sildiroglu, A T Keskin, C C Basekim, E Kizilkaya.
Abstract
Glutaric aciduria or glutaric acidemia type I, an autosomal recessive disease, usually presents with an acute encephalopathic crisis in young children. We report the magnetic resonance (MR) and proton MR spectroscopy (MRS) imaging findings of a previously healthy 20-year-old man who presented with recurrent headaches. Organic acids from the patient's urine contained large amounts of adipate, glutarate, and 3-hydroxyglutarate consistent with glutaric aciduria type I.Entities:
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Year: 2007 PMID: 17520433 DOI: 10.1080/02841850701280874
Source DB: PubMed Journal: Acta Radiol ISSN: 0284-1851 Impact factor: 1.990