Oner Ali Yusuf, Cansu Ali, Akpek Sergin, Serdaroglu Ayse
Department of Radiology, Gazi University School of Medicine, Ankara 06510, Turkey.
Pediatr Radiol. 2007 Oct;37(10):1050-2. doi: 10.1007/s00247-007-0572-4. Epub 2007 Aug 18.
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.
岩藻糖苷贮积症是一种罕见的常染色体隐性溶酶体贮积病,由于α-L-岩藻糖苷酶缺乏,含岩藻糖的糖脂、糖蛋白和寡糖在组织中蓄积。我们报告了一名6岁白种女孩的磁共振成像(MR)表现,该女孩基于从皮肤成纤维细胞分离的互补脱氧核糖核酸(cDNA)被诊断为岩藻糖苷贮积症,其表现为弥漫性白质高信号和苍白球曲线状条纹高信号。本报告还包括磁共振波谱(MRS)结果,即N-乙酰天门冬氨酸/胆碱比值降低以及在3.8 ppm处出现异常峰,这扩展了对这种罕见疾病神经放射学谱的认识。