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Characterization of vertigo and hearing loss in patients with Fabry disease

Abstract Background Fabry Disease (FD) is an X-linked hereditary lysosomal storage disorder which leads to a multisystemic intralysosomal accumulation of globotriaosylceramid (Gb3). Besides prominent renal and cardiac organ involvement, patients commonly complain about vestibulocochlear symptoms lik...

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Principais autores: Maria Köping, Wafaa Shehata-Dieler, Dieter Schneider, Mario Cebulla, Daniel Oder, Jonas Müntze, Peter Nordbeck, Christoph Wanner, Rudolf Hagen, Sebastian P. Schraven
Format: Artigo
Sprog:Inglês
Udgivet: BMC 2018-08-01
Serier:Orphanet Journal of Rare Diseases
Fag:
Fabry disease
Vertigo
VEMP
Cardiomyopathy
Chronic kidney disease
Lysosomal storage disorder
Online adgang:http://link.springer.com/article/10.1186/s13023-018-0882-7
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