Review article
NEUROLOGIC COMPLICATIONS OF ANDERSON-FABRY DISEASE
NEVENA GRBIĆ
; Sestre milosrdnice University Hospital Centre, Department of Neurology, Reference Center for Neuroimmunology and Neurogenetics of the Ministry of Health, Zagreb, Croatia
MILJENKA-JELENA JURAŠIĆ
; Sestre milosrdnice University Hospital Centre, Department of Neurology, Reference Center for Neuroimmunology and Neurogenetics of the Ministry of Health, Zagreb, Croatia
IRIS ZAVOREO
; Sestre milosrdnice University Hospital Centre, Department of Neurology, Reference Center for Neuroimmunology and Neurogenetics of the Ministry of Health, Zagreb, Croatia
LUCIJA ZADRO MATOVINA
; Sestre milosrdnice University Hospital Centre, Department of Neurology, Reference Center for Neuroimmunology and Neurogenetics of the Ministry of Health, Zagreb, Croatia
VANJA BAŠIĆ KES
; Sestre milosrdnice University Hospital Centre, Department of Neurology, Reference Center for Neuroimmunology and Neurogenetics of the Ministry of Health, University of Zagreb, School of Dental Medicine, Zagreb and Josip Juraj Strossmayer University of Osi
Abstract
Introduction: Anderson-Fabry disease is a rare X-linked inborn error and one of the most prevalent lysosomal storage diseases. It is characterized by defi ciency of the lysosomal enzyme
Keywords
Anderson-Fabry disease; neurologic complications; stroke
Hrčak ID:
208627
URI
Publication date:
16.11.2018.
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