Myoclonus in Ataxia-Telangiectasia

被引:9
|
作者
Termsarasab, Pichet [1 ]
Yang, Amy C. [2 ]
Frucht, Steven J. [1 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Neurol, Movement Disorder Div, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA
关键词
Ataxia; myoclonus; telangiectasia; founder mutation;
D O I
10.7916/D88P5Z9X
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Various movement disorders can be found in ataxia-telangiectasia (AT), including ataxia, dystonia, chorea, and myoclonus, but myoclonus has rarely been described as the predominant feature in AT. Case Report: We report two AT patients with prominent myoclonus, illustrating an unusual presentation of this disorder. Sequencing of the ATM gene in the first patient revealed a homozygous truncating mutation, c. 5908C. T (p. Q1970*) in exon 38 of the ATM gene, which has been previously reported as a founder mutation in the Costa Rican population. Discussion: Myoclonus can be a predominant or presenting feature in AT, even without dystonia.
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页数:4
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