Dentatorubral-pallidoluysian atrophy: a case report and review of literature-Reference-Cited by-同舟云学术

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Dentatorubral-pallidoluysian atrophy: a case report and review of literature

Published:2024-09-06 Issue:1 Volume:18 Page:
ISSN:1752-1947
Container-title:Journal of Medical Case Reports
language:en
Short-container-title:J Med Case Reports

Author:

Chen Xin,Xiang Wenwen,Xu Lijun,Zhao Jiahao,Yu Ye,Ke Qing,Liu Zhipeng,Gan Li

Funder

Jiangxi Provincial Natural Science Foundation

The Recruitment Program of Experts of Jiangxi Province

The Science and technology plan of Jiangxi Health Committee

National Natural Science Foundation incubation project of the Second Affiliated Hospital of Nanchang University

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1186/s13256-024-04745-3.pdf

Reference18 articles.

1. Komure O, et al. DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipation. Neurology. 1995;45(1):143–9.

2. Wardle M, Morris HR, Robertson NP. Clinical and genetic characteristics of non-Asian dentatorubral-pallidoluysian atrophy: a systematic review. Mov Disord. 2009;24(11):1636–40.

3. Durr A. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond. Lancet Neurol. 2010;9(9):885–94.

4. Koide R, et al. Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA). Nat Genet. 1994;6(1):9–13.

5. Sunami Y, et al. Radiologic and neuropathologic findings in patients in a family with dentatorubral-pallidoluysian atrophy. AJNR Am J Neuroradiol. 2011;32(1):109–14.

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