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 (ATXN1). In isolated reports of patients with neurological signs [symptomatic patients (SP)], macular abnormalities have been described. However, no repo...

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Detalles Bibliográficos
Autores principales: Ziccardi, Lucia, Cioffi, Ettore, Barbano, Lucilla, Gioiosa, Valeria, Falsini, Benedetto, Casali, Carlo, Parisi, Vincenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8625180/
https://www.ncbi.nlm.nih.gov/pubmed/34830553
http://dx.doi.org/10.3390/jcm10225271

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8625180/
https://www.ncbi.nlm.nih.gov/pubmed/34830553
http://dx.doi.org/10.3390/jcm10225271

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