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岩藻糖苷贮积症:MRI和MRS表现

Fucosidosis: MRI and MRS findings.

作者信息

Oner Ali Yusuf, Cansu Ali, Akpek Sergin, Serdaroglu Ayse

机构信息

Department of Radiology, Gazi University School of Medicine, Ankara 06510, Turkey.

出版信息

Pediatr Radiol. 2007 Oct;37(10):1050-2. doi: 10.1007/s00247-007-0572-4. Epub 2007 Aug 18.

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.

摘要

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。

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