The ratio of alpha-galactosidase to beta-glucuronidase activities in dried blood for the identification of female Fabry disease patients.

  • Z Lukacs
  • A Keil
  • Alfried Kohlschütter
  • M Beck
  • E Mengel

Abstract

Female heterozygous patients with Fabry disease are difficult to identify because of the relatively high residual activity of alpha-galactosidase. We systematically evaluated the activities of various lysosomal enzymes in dried blood samples from Fabry patients and found that the beta-glucuronidase activity was frequently elevated. The ratio of alpha-galactosidase to beta-glucuronidase proved to be a helpful tool for the diagnosis of female Fabry disease patients.

Bibliografische Daten

OriginalspracheDeutsch
Aufsatznummer5
ISSN0141-8955
StatusVeröffentlicht - 2005
pubmed 16151917