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Background
ATXN2 is the causative gene of spinocerebellar ataxia type 2 (SCA2) and has been implicated in glaucoma pathogenesis. Therefore, studying ocular changes in SCA2 could uncover clinically relevant changes.
Objective
The aim was to investigate optic disc and retinal architecture in SCA2.
Methods
We evaluated 14 patients with SCA2 and 26 controls who underwent intraocular pressure measurement,...
Background
Neurodegeneration affects the brain and peripheral nervous system in spinocerebellar ataxia type 3 (SCA3). As the retina is also involved, studying the retinal architecture in a cohort of patients could reveal clinically relevant biomarkers.
Objective
The aim is to investigate retinal architecture in SCA3 to identify potential biomarkers.
Methods
We evaluated 38 patients with SCA3...
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