Literature DB >> 1654042

Chemical diagnosis of Fabry's disease by fluorometric assay and fast atom bombardment/mass spectrometry.

T Nakanishi1, S Funahashi, T Funai, T Hashimoto, A Shimizu.   

Abstract

We report the results of a fluorometric assay for alpha-galactosidase A (EC.3.2.1.22) in plasma and leukocytes, and fast atom bombardment/mass spectrometry (FAB/MS) analysis of glycosphingolipids in urine sediments from a patient with Fabry's disease. In plasma, this patient had only 5.0% of the normal amount of alpha-galactosidase A, and his brother and mother had 11.0% and 25.0%, respectively. In leukocytes, the activities were below 8.0%. Glycosphingolipids from urine sediments were partially purified using a Sep-Pack C18 cartridge. The chemical diagnosis of Fabry's disease can be made more rapidly and accurately using fluorometric and FAB/MS analyses.

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Year:  1991        PMID: 1654042     DOI: 10.1177/000456329102800410

Source DB:  PubMed          Journal:  Ann Clin Biochem        ISSN: 0004-5632            Impact factor:   2.057


  1 in total

1.  Monitoring enzyme replacement therapy in Fabry disease--role of urine globotriaosylceramide.

Authors:  P D Whitfield; J Calvin; S Hogg; E O'Driscoll; D Halsall; K Burling; G Maguire; N Wright; T M Cox; P J Meikle; P B Deegan
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.982

  1 in total

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