Split hand and minipolymyoclonus in spinocerebellar ataxia type 3: a case report

Split hand and minipolymyoclonus in spinocerebellar ataxia type 3: a case report

Abstract Background Spinocerebellar ataxia type 3 (SCA3), also known as Machado–Joseph disease, is an autosomal dominant neurodegenerative disorder caused by CAG repeat expansion in exon 10 of ATXN3. Extra-cerebellar manifestations, including external ophthalmoplegia, dystonia, Parkinsonism, and per...

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Main Authors: Anli Eki, Atsuhiko Sugiyama, Kazumoto Shibuya, Yuki Nakagawa, Takayuki Ishige, Tomoki Suichi, Ryo Otani, Satoshi Kuwabara
Format: Article
Language:English
Published: BMC 2024-11-01
Series:BMC Neurology
Subjects:
Myoclonus
Spinocerebellar ataxias
Multiple system atrophy
Short-interval intracortical inhibition
Voxel-based morphometry
Online Access:https://doi.org/10.1186/s12883-024-03948-x
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https://doi.org/10.1186/s12883-024-03948-x

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