Glycolipid and mucopolysaccharide abnormality in fibroblasts of fabry's disease
- PMID: 4239585
- DOI: 10.1126/science.164.3887.1522
Glycolipid and mucopolysaccharide abnormality in fibroblasts of fabry's disease
Abstract
Cultures of skin fiibroblasts from a patient with Fabry's disease showed an accumulation of the glycolipid, galactosyl-galactosyl-glucosyl ceramide. Such cells also showed metachromasia on staining with toluidine blue and a markedly elevated acid mucopolysaccharide content.
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