Suppr超能文献

产前黏多糖贮积症II型(亨特综合征)神经系统的形态学观察

Morphological observations in the nervous system of prenatal mucopolysaccharidosis II (M. Hunter).

作者信息

Meier C, Wismann U, Herschkowitz N, Bischoff A

出版信息

Acta Neuropathol. 1979 Nov;48(2):139-43. doi: 10.1007/BF00691155.

Abstract

Light and electron microscopic finding in the nervous system of a 23-week-old fetus are reported, in which MPS II was diagnosed prenatally. The degrees of myelination and neuronal differentiation were similar as in a normal fetus of the same age. A storage of mucopolysaccharides in typical vacuolar inclusion bodies was present throughout the peripheral and central nervous system, mainly in cells of mesenchymal origin. "Zebra" bodies and granulo-membranous bodies, which are thought to represent secondard ganglioside accumulation were only found in the well developed neurons of the spinal cord and spinal ganglia, but not in the poorly developed neurons of the cerebellar and cerebral cortex. Mucopolysaccharide storage in endothelial cells of cerebral bood vessels precedes the appearance of lipid storgae in cerebral neurons.

摘要

报道了一名23周龄胎儿神经系统的光镜和电镜检查结果,该胎儿在产前被诊断为黏多糖贮积症II型。髓鞘形成和神经元分化程度与同龄正常胎儿相似。在整个外周和中枢神经系统中,主要在间充质来源的细胞中存在典型空泡包涵体内的黏多糖贮积。被认为代表继发性神经节苷脂蓄积的“斑马”体和颗粒膜体仅在脊髓和脊神经节发育良好的神经元中发现,而在小脑和大脑皮质发育不良的神经元中未发现。脑血管内皮细胞中的黏多糖贮积先于脑神经元中脂质贮积的出现。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验