Authors: Florian M Barras Raphaël Maire
Publish Date: 2006/03/07
Volume: 263, Issue: 7, Pages: 688-691
Abstract
Fabry’s disease is a chromosomal Xlinked inherited disease which causes a lack of the lysosomal alphagalactosidase A enzyme leading to a cellular accumulation of glycosphingolipids This accumulation leads to various clinical disorders including inner ear lesions with sensorineural hearing loss and dizziness This article proposes to describe a clinical case of a patient suffering from Fabry’s disease with inner ear associated problems and to review the literature focusing on this subject
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