Cognitive impairment and Fabry Disease: a case report with mutation S126G

Anderson-Fabry Disease is a lysosomal storage disease, multisystem, progressive, hereditary, linked to the X-chromosome. Specifically, it is characterized by a glycosphingolipid metabolism due to the reduction or absence of Alpha-galactosidase, an enzyme activity lisosomile gene mutation GLA (X...

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Bibliographic Details

Published in:	Neuropsychological Trends
Main Authors:	Razza, Grazia, Spadaro, Daniela, Giordano, Antonello, Scalia, Simone, Colomba, Paolo, Zizzo, Carmela, Duro, Giovanni, Iemolo, Francesco
Format:	Article
Language:	English
Published:	LED Edizioni Universitarie 2016-11-01
Subjects:	Fabry Cognitive deficit Stroke
Online Access:	http://www.ledonline.it/NeuropsychologicalTrends/allegati/NeuropsychologicalTrends_20_Razza.pdf