| Literature DB >> 16151917 |
Z Lukacs1, A Keil, A 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.Entities:
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Year: 2005 PMID: 16151917 DOI: 10.1007/s10545-005-0039-4
Source DB: PubMed Journal: J Inherit Metab Dis ISSN: 0141-8955 Impact factor: 4.982