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Retinal hyperreflective foci in Fabry disease
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. METHODS...
Autores principales: | Atiskova, Yevgeniya, Rassuli, Rahman, Koehn, Anja Friederike, Golsari, Amir, Wagenfeld, Lars, du Moulin, Marcel, Muschol, Nicole, Dulz, Simon |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933914/ https://www.ncbi.nlm.nih.gov/pubmed/31878969 http://dx.doi.org/10.1186/s13023-019-1267-2 |
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