Review article

DIAGNOSIS OF ANDERSON-FABRY DISEASE

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
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

Abstract

Introduction: Anderson- Fabry disease is one of the most common lysosomal storage diseases (after Gaucher disease). It is an X-linked inborn error. A disease is characterized by defi ciency of the lysosomal enzyme

Keywords

Anderson-Fabry disease; diagnosis; screening; stroke

Hrčak ID:

208626

URI

https://hrcak.srce.hr/208626

Publication date:

16.11.2018.

Article data in other languages: croatian

Visits: 4.845 *