| Literature DB >> 20655779 |
J H van der Kolk1, I D Wijnberg, C M Westermann, L Dorland, M G M de Sain-van der Velden, L C Kranenburg, M Duran, J A Dijkstra, J J van der Lugt, R J A Wanders, E Gruys.
Abstract
This case-series describes fourteen horses suspected of equine acquired multiple acyl-CoA dehydrogenase deficiency (MADD) also known as atypical myopathy of which seven cases were confirmed biochemically with all horses having had access to leaves of the Maple tree (Acer pseudoplatanus) covered with European tar spot (Rhytisma acerinum). Assessment of organic acids, glycine conjugates, and acylcarnitines in urine was regarded as gold standard in the biochemical diagnosis of equine acquired multiple acyl-CoA dehydrogenase deficiency.Entities:
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Year: 2010 PMID: 20655779 DOI: 10.1016/j.ymgme.2010.06.019
Source DB: PubMed Journal: Mol Genet Metab ISSN: 1096-7192 Impact factor: 4.797