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[GM1神经节苷脂贮积症。两例临床、放射学、生物化学及组织学研究(作者译)]

[Gangliosidosis GM1. Clinical, radiologic, biochemical and histological studies in two cases (author's transl)].

作者信息

Roche Herrero M C, Pascual Castroviejo I, Leroy J G, González Sastre F, Gutiérrez M

出版信息

An Esp Pediatr. 1977 Apr;10(4):405-12.

PMID:406824
Abstract

Two cases of Gangliosidosis GM1 are presented. They are a child who showed psychomotor backward and generalized osteoporosis, died at 16 months, and a girl studied because of psychomotor backward when she was less than a year. This girl showed radiological vertebrae alterations similar to mucopolysaccharidosis and died when she was 7 years old. The enzymatic determinations in serum and cultured fibroblasts showed beta-galactosidase deficiency in both cases. Important storage of cerebral gangliosides with increase of the percentage of GM1 was also found in both cases. Histological alterations were found in some other organs besides the brain.

摘要

本文报告了2例GM1神经节苷脂贮积症。其中1例为儿童,表现为精神运动发育迟缓及全身性骨质疏松,16个月时死亡;另1例为女孩,不到1岁时因精神运动发育迟缓接受检查,其影像学显示脊椎改变类似于黏多糖贮积症,7岁时死亡。血清及培养的成纤维细胞酶学检测显示,2例均存在β-半乳糖苷酶缺乏。2例均发现脑内神经节苷脂大量蓄积,GM1百分比增加。除脑外,在其他一些器官也发现了组织学改变。

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