Spinocerebellar Ataxia Type 8 as a Huntington’s Disease-like Syndrome (P6-5.019)

To describe an atypical presentation of spinocerebellar ataxia type 8 (SCA8) with chorea, and how this impacts workup of Huntington’s disease (HD)-like syndromes.

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Publication Details

Journal
Neurology
Published
2025-04-07
DOI
https://doi.org/10.1212/wnl.0000000000208589
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.00
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article

Spinocerebellar Ataxia Type 8 as a Huntington’s Disease-like Syndrome (P6-5.019)

Sean Lee, S. K. Bose
1 links
Neurology
Genetic Neurodegenerative Diseases
article

Spinocerebellar Ataxia Type 8 as a Huntington’s Disease-like Syndrome (P6-5.019)

Sean Lee, S. K. Bose
article en

Abstract

To describe an atypical presentation of spinocerebellar ataxia type 8 (SCA8) with chorea, and how this impacts workup of Huntington’s disease (HD)-like syndromes.

NeurologyVol. 104(7_Supplement_1)
University of Arizona (US)
Good health and well-being
Openalex Percentile: Top 92%
Genetic Neurodegenerative Diseases
DOISourceOpenAlex
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Spinocerebellar Ataxia Type 8 as a Huntington’s Disease-like Syndrome (P6-5.019) — Sean Lee, S. K. Bose · Neurology (2025) | TGRS Research Map | TGRS