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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


Full text: croatian pdf 741 Kb

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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

https://hrcak.srce.hr/89625

Publication date:

1.3.2011.

Article data in other languages: croatian

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