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用于杂聚糖代谢紊乱的尿液筛查。一个综合系统十年经验的结果。

Urinary screening for disorders of heteroglycan metabolism. Results of 10 years experience with a comprehensive system.

作者信息

Sewell A C

机构信息

Universitäts-Kinderklinik Mainz.

出版信息

Klin Wochenschr. 1988 Jan 15;66(2):48-53. doi: 10.1007/BF01713010.

Abstract

The results of 10 years experience in urinary screening for disorders of heteroglycan metabolism are presented. Over 5,000 urines were analysed of which 216 were positive for excess mucopolysacchariduria. The enzymatic diagnosis was achieved in 159 mucopolysaccharidoses of which Type III Sanfilippo was the commonest (86 cases), followed by Type II Hunter (31 cases) and Type I Hurler (21 cases). A total of 27 urines were positive for excess oligosacchariduria, the enzymatic diagnosis being established in 20 cases. The most frequently encountered oligosaccharidosis was GM1 gangliosidosis (10 cases), followed by mannosidosis (5 cases). No cases of fucosidosis were found.

摘要

本文介绍了10年来对异聚糖代谢紊乱进行尿液筛查的经验结果。共分析了5000多份尿液,其中216份黏多糖尿过多呈阳性。对159例黏多糖贮积症进行了酶学诊断,其中Ⅲ型Sanfilippo最常见(86例),其次是Ⅱ型Hunter(31例)和Ⅰ型Hurler(21例)。共有27份尿液低聚糖尿过多呈阳性,其中20例进行了酶学诊断。最常见的低聚糖贮积症是GM1神经节苷脂贮积症(10例),其次是甘露糖苷贮积症(5例)。未发现岩藻糖苷贮积症病例。

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