Retinal hyperreflective foci in Fabry disease

Retinal hyperreflective foci in Fabry disease

Abstract Background Fabry disease (FD) is an X-linked inherited storage disorder caused by deficiency of lysosomal alpha-Galactosidase A. Here we describe new retinal findings in patients with FD assessed by Spectral domain optical coherence tomography (SD-OCT) and their possible clinical relevance....

Full description

Bibliographic Details
Main Authors: Yevgeniya Atiskova, Rahman Rassuli, Anja Friederike Koehn, Amir Golsari, Lars Wagenfeld, Marcel du Moulin, Nicole Muschol, Simon Dulz
Format: Article
Language:English
Published: BMC 2019-12-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Fabry disease
SD-OCT
Retina
Hyperreflective foci
Vessel tortuosity
Online Access:https://doi.org/10.1186/s13023-019-1267-2

Internet

https://doi.org/10.1186/s13023-019-1267-2

Similar Items