Sewell A C
Clin Chem. 1981 Feb;27(2):243-5.
I describe a simple set of procedures for the screening of patients' urine to detect oligosaccharide-storage diseases. Urines from patients with mucolipidosis I, mannosidosis, fucosidosis, aspartylglycosaminuria, and type VI glycogen-storage disease can be distinguished by thin-layer chromatography. Patients with beta-galactosidase deficiency can be detected by use of a combination of ion-exchange and thin-layer chromatography. Excess sialyloligosaccharide excretion is detected by using gel filtration and a quantitative assay for neuraminic acid. The advantages of the system are detection of virtually all known disorders in which oligosaccharides are over-excreted, production of characteristic patterns, and small sample requirement.
我描述了一套简单的程序,用于筛查患者尿液以检测寡糖贮积病。通过薄层色谱法可区分黏脂贮积症I型、甘露糖苷贮积症、岩藻糖苷贮积症、天冬氨酰葡萄糖胺尿症和VI型糖原贮积病患者的尿液。使用离子交换和薄层色谱相结合的方法可检测β-半乳糖苷酶缺乏症患者。通过凝胶过滤和对神经氨酸的定量测定来检测唾液酸寡糖排泄过多的情况。该系统的优点是几乎能检测出所有已知的寡糖过度排泄的疾病,产生特征性图谱,且对样本需求量小。