首页> 美国卫生研究院文献>The Journal of Neurology and Psychopathology >Pontine atrophy precedes cerebellar degeneration in spinocerebellar ataxia 7: MRI-based volumetric analysis
【2h】

Pontine atrophy precedes cerebellar degeneration in spinocerebellar ataxia 7: MRI-based volumetric analysis

机译:桥性肌萎缩先于脊髓小脑共济失调小脑变性7:基于MRI的体积分析

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

>Background and objective: Spinocerebellar ataxia 7 (SCA7) is characterised by cerebellar ataxia and visual loss. The aim of the present study was to elucidate the magnetic resonance imaging (MRI) findings characteristic of patients with SCA7. >Methods: Twenty patients with SCA (eight SCA3, three SCA6, and nine SCA7) and 20 control subjects underwent an MRI-based volumetric analysis. >Results: The pontine volume in patients with SCA7 was decreased by a greater amount than in patients with other types of SCA (p<0.01), whereas the cerebellar volume was not different from that in other types of SCA (p>0.05). Pontine atrophy was a consistent finding in all patients with SCA7 regardless of the degree of cerebellar atrophy or the severity or duration of illness. In contrast, cerebellar atrophy was not found in those with a short duration of illness or mild ataxia, but became prominent as the severity and duration of illness progressed. >Conclusions: Our study suggests that neurodegeneration is ongoing during the life of individuals with SCA7, and that the primary pathology in these individuals involves the brainstem rather than the cerebellum. In addition, pontine atrophy is a prominent, consistent finding in SCA7, and may help in establishing the clinical diagnosis of SCA7.
机译:>背景和目的:脊髓小脑性共济失调7(SCA7)的特征是小脑性共济失调和视力减退。本研究的目的是阐明SCA7患者的磁共振成像(MRI)发现特征。 >方法:对20例SCA患者(8例SCA3、3例SCA6和9例SCA7)和20例对照受试者进行了基于MRI的容量分析。 >结果:与其他类型的SCA患者相比,SCA7患者的脑桥体积减少幅度更大(p <0.01),而小脑的体积与其他类型的SCA患者无差异(p> 0.05)。在所有SCA7患者中,无论小脑萎缩程度,疾病的严重程度或持续时间如何,庞汀萎缩都是一致的发现。相反,在疾病持续时间短或轻度共济失调的患者中未发现小脑萎缩,但随着疾病的严重程度和持续时间的发展,小脑萎缩变得尤为突出。 >结论:我们的研究表明,在SCA7患者的一生中,神经退行性疾病仍在持续,并且这些患者的主要病理学涉及脑干而不是小脑。此外,桥脑萎缩是SCA7中一个突出的,一致的发现,可能有助于建立SCA7的临床诊断。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号