Macular Morpho-Functional and Visual Pathways Functional Assessment in Patients with Spinocerebellar Type 1 Ataxia with or without Neurological Signs

Spinocerebellar ataxia type 1 (SCA-ATXN1) is an autosomal dominant, neurodegenerative disease, caused by CAG repeat expansion in the ataxin-1 gene (<i>ATXN1</i>). In isolated reports of patients with neurological signs [symptomatic patients (SP)], macular abnormalities have been describe...

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Bibliographic Details
Main Authors: Lucia Ziccardi, Ettore Cioffi, Lucilla Barbano, Valeria Gioiosa, Benedetto Falsini, Carlo Casali, Vincenzo Parisi
Format: Article
Language:English
Published: MDPI AG 2021-11-01
Series:Journal of Clinical Medicine
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Online Access:https://www.mdpi.com/2077-0383/10/22/5271