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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


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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

https://hrcak.srce.hr/208627

Publication date:

16.11.2018.

Article data in other languages: croatian

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