Review article
ANDERSON-FABRY DISEASE AND RENAL TRANSPLANTATION
NIKOLINA BAŠIĆ-JUKIĆ
; Zagreb University Hospital Center and School of Medicine, University of Zagreb, Department of Nephrology, Arterial Hypertension and Dialysis Zagreb, Croatia
PETAR KES
; Zagreb University Hospital Center and School of Medicine, University of Zagreb, Department of Nephrology, Arterial Hypertension and Dialysis Zagreb, Croatia
TVRTKO HUDOLIN
; Zagreb University Hospital Center, Department of Urology, Zagreb, Croatia
INES MESAR
; Zagreb University Hospital Center and School of Medicine, University of Zagreb, Department of Nephrology, Arterial Hypertension and Dialysis Zagreb, Croatia
MARIJANA ĆORIĆ
; Zagreb University Hospital Center, Department of Pathology, Zagreb, Croatia
ŽELJKO KAŠTELAN
; Zagreb University Hospital Center, Department of Urology, Zagreb, Croatia
Abstract
Anderson-Fabry disease is a rare disease associated with progressive accumulation of globotriaosylceramide in visceral organs and vascular endothelium. The disease primarily affects male patients. It has long been considered that females are asymptomatic carriers of Anderson-Fabry disease. However, recent results demonstrated a significant proportion of symptomatic affected females. We present our experience in the treatment of patients with Anderson-Fabry disease having received allograft from deceased donor, as well as follow-up of patients having received allograft from donor with unrecognized Anderson-Fabry disease.
Keywords
Anderson-Fabry disease; renal transplantation; outcome
Hrčak ID:
89625
URI
Publication date:
1.3.2011.
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