Evolution of renal pathology in Fabry disease.

Abstract

UNLABELLED Fabry disease is a rare lysosomal storage disorder which results from deficient activity of the enzyme alpha-galactosidase A. The resultant deposition and progressive accumulation of glycosphingolipids in all types of body tissue leads to severe clinical manifestations involving the heart, CNS and kidney. Renal manifestations are observed… (More)

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@article{Sessa2003EvolutionOR, title={Evolution of renal pathology in Fabry disease.}, author={Adalberto Sessa and Mietta Meroni and Graziana Battini and Marco Righetti and Manuela Nebuloni and Antonella Tosoni and Gian Luca Vago}, journal={Acta paediatrica (Oslo, Norway : 1992). Supplement}, year={2003}, volume={92 443}, pages={6-8; discussion 5} }