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本文引用的文献

1
Door-to-door survey of major neurological disorders in Al Kharga District, New Valley, Egypt: methodological aspects.埃及新河谷省阿尔哈加尔地区主要神经障碍的逐户调查:方法学方面。
Neuroepidemiology. 2010;35(3):185-90. doi: 10.1159/000314345. Epub 2010 Jul 24.
2
Sporadic ataxia with adult onset: classification and diagnostic criteria.散发性成年发病的共济失调:分类和诊断标准。
Lancet Neurol. 2010 Jan;9(1):94-104. doi: 10.1016/S1474-4422(09)70305-9.
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[Hereditary ataxias].[遗传性共济失调]
Tidsskr Nor Laegeforen. 2008 Sep 11;128(17):1977-80.
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Age-specific reference ranges for polychlorinated biphenyls (PCB) based on the NHANES 2001-2002 survey.基于2001 - 2002年美国国家健康与营养检查调查(NHANES)的多氯联苯(PCB)特定年龄参考范围。
J Toxicol Environ Health A. 2007 Nov;70(21):1873-7. doi: 10.1080/15287390701457688.
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Cerebral palsy in Norway: prevalence, subtypes and severity.挪威的脑瘫:患病率、亚型及严重程度。
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An approach to the patient with late-onset cerebellar ataxia.迟发性小脑共济失调患者的诊疗方法。
Nat Clin Pract Neurol. 2006 Nov;2(11):629-35; quiz 1 p following 635. doi: 10.1038/ncpneuro0319.
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Cerebellar ataxia and central nervous system whipple disease.小脑性共济失调与中枢神经系统惠普尔病
Arch Neurol. 2005 Apr;62(4):618-20. doi: 10.1001/archneur.62.4.618.
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9
CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia.TATA盒结合蛋白基因中的CAG重复序列扩增导致常染色体显性遗传性小脑共济失调。
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Rehabilitation of cerebral palsy in a developing country: the need for comprehensive assessment.发展中国家的脑瘫康复:全面评估的必要性。
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基于人群的埃及新谷省阿尔卡arga 地区获得性小脑共济失调研究。

Population-based study of acquired cerebellar ataxia in Al-Kharga district, New Valley, Egypt.

机构信息

Department of Neurology and Psychiatry, Assiut University, Assiut, Egypt;

出版信息

Neuropsychiatr Dis Treat. 2011;7:183-7. doi: 10.2147/NDT.S14497. Epub 2011 Apr 5.

DOI:10.2147/NDT.S14497
PMID:21552320
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3083991/
Abstract

BACKGROUND

The aim of this research was to determine the prevalence and etiology of acquired ataxia in Al-Kharga district, New Valley, Egypt.

METHODS

A population-based study of acquired ataxia was conducted in a defined geographical region with a total population of 62,583. A door-to-door survey was used to identify cases of acquired cerebellar ataxia. Patients with acquired cerebellar ataxia at any age and of both genders were included. Cases of known inherited cerebellar ataxia, acquired neurological disorders with ataxia as a minor feature, or pure acquired sensory ataxia, were excluded.

RESULTS

We identified 17 cases of acquired ataxia, of which eight were vascular, six were an ataxic cerebral palsy subtype, and three involved postencephalitic ataxia. The crude prevalence rate for acquired ataxia was 27.16/100,000 (95% confidence interval [CI]: 14.3-40.1). The mean age of the patients at interview was 31.8 (range 4-72) years, with a male to female ratio of 2.1:1. The most frequent presenting complaint was disturbance of gait (90.7%). The majority (92%) were ambulatory, but only 9.3% were independently self-caring.

CONCLUSION

This population-based study provides an insight into acquired cerebellar ataxia within a defined region, and may inform decisions about the rational use of health care resources for patients with acquired cerebellar ataxia. The most common causes of acquired cerebellar ataxia in this region were cerebrovascular injury and cerebral palsy.

摘要

背景

本研究旨在确定埃及新谷省阿尔-卡赫拉地区获得性共济失调的患病率和病因。

方法

在一个总人口为 62583 人的特定地理区域进行了一项基于人群的获得性共济失调研究。采用挨家挨户的方式来确定获得性小脑共济失调的病例。本研究纳入了任何年龄和性别的获得性小脑共济失调患者。已知遗传性小脑共济失调、以共济失调为次要特征的获得性神经障碍或单纯获得性感觉共济失调的病例除外。

结果

我们共发现了 17 例获得性共济失调患者,其中 8 例为血管性共济失调,6 例为共济失调型脑瘫,3 例为脑炎后共济失调。获得性共济失调的粗患病率为 27.16/100,000(95%置信区间[CI]:14.3-40.1)。患者在接受采访时的平均年龄为 31.8 岁(范围为 4-72 岁),男女比例为 2.1:1。最常见的首发症状是步态紊乱(90.7%)。大多数(92%)患者可步行,但仅有 9.3%可独立自理。

结论

本基于人群的研究深入了解了特定区域内的获得性小脑共济失调,可为合理利用卫生保健资源治疗获得性小脑共济失调患者提供依据。该地区获得性小脑共济失调的最常见病因是脑血管损伤和脑瘫。