Prominent Oromandibular Dystonia and Pharyngeal Telangiectasia in Atypical Ataxia Telangiectasia

被引:28
作者
Carrillo, Fatima [1 ,2 ]
Schneider, Susanne A. [1 ,3 ]
Taylor, A. Malcolm R. [4 ]
Srinivasan, Venkataramanan [4 ]
Kapoor, Raj [3 ]
Bhatia, Kailash P. [1 ,3 ]
机构
[1] UCL, Inst Neurol, Sobell Dept Motor Neurosci & Movement Disorders, London WC1N 3BG, England
[2] HH UU Virgen Rocio, Serv Neurol, Seville, Spain
[3] Natl Hosp Neurol & Neurosurg, London WC1N 3BG, England
[4] Univ Birmingham, CR UK Inst Canc Studies, Birmingham B15 2TT, W Midlands, England
关键词
Dystonia; Ataxia telangiectasia; Atypical presentation; ATM protein; Radiosensitivity; Oromandibular/oro-bulbar; STRAND BREAK REPAIR; ATM GENE; INDIVIDUALS; PHENOTYPE; FEATURES; LINKAGE; PROTEIN;
D O I
10.1007/s12311-008-0055-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Ataxia telangiectasia (A-T) typically presents with early-onset progressive cerebellar ataxia, oculomotor apraxia and later, oculo-cutaneous telangiectasia. Extrapyramidal symptoms, apart from chorea, are rare. In this paper, we report a case of A-T with an atypically mild and slowly progressive disease course. Although by history there was mild gait clumsiness in early childhood, the leading problem was that of dystonia with onset at age 15, in the absence of gross gait imbalance or ocular motor apraxia. Dystonia was generalized and with prominent oromandibular involvement. Unusually, a leash of telangiectasia was present on the posterior pharyngeal wall, while other features frequently associated with A-T were absent.
引用
收藏
页码:22 / 27
页数:6
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