Renal pathological changes in Fabry disease

Fabry disease is a rare X‐linked disorder, characterized by deficient activity of the lysosomal enzyme α‐galactosidase A. This leads to systemic accumulation of the glycosphingolipid globotriaosylceramide (Gb3) in all body tissues and organs, including the kidney. Renal manifestations are less evide...

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Veröffentlicht in:	Journal of inherited metabolic disease 2001-01, Vol.24 (S2), p.66-70
Hauptverfasser:	Sessa, A., Meroni, M., Battini, G., Maglio, A., Brambilla, P. L., Bertella, M., Nebuloni, M., Pallotti, F., Giordano, F., Bertagnolio, B., Tosoni, A.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Disease Progression Errors of metabolism Fabry Disease - complications Fabry Disease - pathology Fabry Disease - physiopathology Female Humans Kidney - pathology Kidney - physiopathology Kidney Diseases - etiology Kidney Diseases - pathology Kidney Diseases - therapy Lipids (lysosomal enzyme disorders, storage diseases) Male Medical sciences Metabolic diseases
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