Pregledni rad

ANDERSON-FABRY DISEASE AND RENAL TRANSPLANTATION

NIKOLINA BAŠIĆ-JUKIĆ ; Klinički bolnički centar Zagreb, Medicinski fakultet Sveučilišta u Zagrebu, Zavod za nefrologiju, arterijsku hipertenziju i dijalizu, Zagreb, Hrvatska
PETAR KES ; Klinički bolnički centar Zagreb, Medicinski fakultet Sveučilišta u Zagrebu, Zavod za nefrologiju, arterijsku hipertenziju i dijalizu, Zagreb, Hrvatska
TVRTKO HUDOLIN ; Klinički bolnički centar Zagreb, Klinika za urologiju, Zagreb, Hrvatska
INES MESAR ; Klinički bolnički centar Zagreb, Medicinski fakultet Sveučilišta u Zagrebu, Zavod za nefrologiju, arterijsku hipertenziju i dijalizu, Zagreb, Hrvatska
MARIJANA ĆORIĆ ; Klinički bolnički centar Zagreb, Zavod za patologiju, Zagreb, Hrvatska
ŽELJKO KAŠTELAN ; Klinički bolnički centar Zagreb, Klinika za urologiju, Zagreb, Hrvatska

Sažetak

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.

Ključne riječi

Anderson-Fabry disease; renal transplantation; outcome

Hrčak ID:

89625

URI

https://hrcak.srce.hr/89625

Datum izdavanja:

1.3.2011.

Podaci na drugim jezicima: hrvatski

Posjeta: 1.272 *