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Article

The association between diplopia and clinical phenotypes in spinocerebellar ataxia type 3.

BMC neurology - 10 Apr 2026

Zheng Mei, Cui Mao-Lin, Lin Wei, Huang Zhuo-Ying, Cai Bin, Gan Shi-Rui

Abstract excerpt

BACKGROUND: Spinocerebellar ataxia type 3 (SCA3) is a rare monogenic hereditary neurodegenerative disease. It is the most common form of spinocerebellar ataxia worldwide, with diplopia being one of its most frequent symptoms. Diplopia has been reported to be associated with clinical phenotypes and daily living activities in various neurodegenerative diseases. OBJECTIVES: Our objective is to investigate the...

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PMID: 41963867
DOI: 10.1186/s12883-026-04848-y
PMCID: PMC13188680

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

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