Tamagawa K, Morimatsu Y, Fujisawa K, Hara A, Taketomi T
Brain Dev. 1985;7(6):599-609. doi: 10.1016/s0387-7604(85)80008-5.
Pathological and biochemical studies of two sibling cases (18-year-old girl and 16-year-old boy) with Sanfilippo syndrome type B are presented. Pathological study revealed distended neurons and neuronal processes with inclusions throughout the CNS and the visceral organs, and neuronal loss and corresponding gliosis. The authors paid particular attention to atrophic changes in the thalamus and to "dissociation gliomyélinique" in the cerebral white matter. Histochemistry and electron microscopy revealed regional differences in stored materials. Biochemical studies revealed an accumulation of glycosaminoglycans in the CNS and abnormalities in the lipid metabolism in the brain and visceral organs. A protein assay of the cerebrum showed increased glial fibrillary acidic protein and low levels of myelin basic protein in the white matter.
本文介绍了两例B型Sanfilippo综合征同胞病例(一名18岁女孩和一名16岁男孩)的病理和生化研究。病理研究显示,整个中枢神经系统和内脏器官中神经元和神经突扩张并伴有包涵体,以及神经元丢失和相应的胶质增生。作者特别关注丘脑的萎缩性变化以及脑白质中的“脱髓鞘性胶质变性”。组织化学和电子显微镜检查揭示了储存物质的区域差异。生化研究显示中枢神经系统中糖胺聚糖的积累以及脑和内脏器官中脂质代谢的异常。大脑蛋白质分析显示白质中胶质纤维酸性蛋白增加而髓鞘碱性蛋白水平降低。