| Literature DB >> 17704911 |
Ali Yusuf Oner1, Ali Cansu, Sergin Akpek, Ayse Serdaroglu.
Abstract
Fucosidosis is a rare, autosomal recessive lysosomal storage disease in which fucose-containing glycolipids, glycoproteins, and oligosaccharides accumulate in tissues as a consequence of alpha-L: -fucosidase enzyme deficiency. We present the MR imaging findings of diffuse white-matter hyperintensity and pallidal curvilinear streak hyperintensity in a 6-year-old Caucasian girl with a diagnosis of fucosidosis based on cDNA isolated from skin fibroblasts. This report also includes the MRS findings of a decreased N-acetylaspartate/choline ratio together with an abnormal peak at 3.8 ppm which expand the knowledge of the neuroradiological spectrum of this rare disease.Entities:
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Year: 2007 PMID: 17704911 DOI: 10.1007/s00247-007-0572-4
Source DB: PubMed Journal: Pediatr Radiol ISSN: 0301-0449