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三十七例伴有异常头位、眼球震颤和斜视儿童的眼震电图及临床特征:一种临床算法的基础

Oculographic and clinical characterization of thirty-seven children with anomalous head postures, nystagmus, and strabismus: the basis of a clinical algorithm.

作者信息

Hertle R W, Zhu X

机构信息

Laboratory of Sensorimotor Research and the National Eye Institute, the National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

J AAPOS. 2000 Feb;4(1):25-32. doi: 10.1016/s1091-8531(00)90008-9.

Abstract

BACKGROUND AND PURPOSE

We studied children with nystagmus who also had anomalous head postures and strabismus to determine the etiology of the conditions and present a diagnostic clinical algorithm.

METHODS

The patients for this study were among the 560 patients evaluated in the ocular motor neurophysiology laboratory between the years 1991 and 1997. Clinical characteristics, infrared oculography data, and medical and surgical treatments were entered into a database for analysis. Oculography was performed on all patients according to a standard protocol, and data were stored and analyzed off-line. Etiology of anomalous head posture was determined with both clinical and oculography information.

RESULTS

Thirty-seven children are the subjects of this report. The etiology of anomalous head posture was a "gaze null" due to congenital nystagmus in 23 (62%) patients, an "adduction null" due to manifest latent nystagmus in 12 (32%) patients, spasmus nutans in 1 (3%) patient, and strabismus in 1 (3%) patient. The patients' ages ranged from 9 months to 12 years and averaged 4.4 years. Sixty-nine percent were male patients. Nineteen (63%) of 30 patients had abnormal recognition (linear optotype) acuity in at least 1 eye on monocular cover; the recognition remained abnormal in 5 (17%) of 30 patients under binocular conditions. Thirty percent of patients had amblyopia, 16% had some structural disease of the eyes, 22% had some systemic syndrome or abnormality, 57% had a significant refractive error, and 27% had some ability to fuse.

CONCLUSIONS

The major etiology for anomalous head posture in these patients was to adopt a gaze null due to congenital nystagmus (62% of patients) regardless of the direction of their anomalous head posture or type of strabismus. Moving the fixing eye as the first step for the anomalous head posture, combined with moving the nonfixing eye for the resulting strabismus may help treat these patients.

摘要

背景与目的

我们对患有眼球震颤、异常头位和斜视的儿童进行了研究,以确定这些病症的病因,并提出一种诊断临床算法。

方法

本研究的患者来自1991年至1997年间在眼动神经生理学实验室接受评估的560名患者。将临床特征、红外眼动图数据以及药物和手术治疗情况录入数据库进行分析。所有患者均按照标准方案进行眼动图检查,数据存储后进行离线分析。根据临床和眼动图信息确定异常头位的病因。

结果

本报告以37名儿童为研究对象。异常头位的病因中,23名(62%)患者是由于先天性眼球震颤导致的“注视零点”,12名(32%)患者是由于显性潜伏性眼球震颤导致的“内收零点”,1名(3%)患者是痉挛性斜颈,1名(3%)患者是斜视。患者年龄从9个月至12岁不等,平均4.4岁。69%为男性患者。30名患者中有19名(63%)在单眼遮盖时至少一只眼睛的识别(线性视标)视力异常;在双眼条件下,30名患者中有5名(17%)的识别仍异常。30%的患者有弱视,16%有眼部某些结构疾病,22%有某些全身综合征或异常,57%有明显屈光不正,27%有一定融合能力。

结论

这些患者异常头位的主要病因是先天性眼球震颤导致的注视零点(62%的患者),无论其异常头位方向或斜视类型如何。将固定眼移动作为异常头位的第一步,再结合移动非固定眼以治疗由此产生的斜视,可能有助于治疗这些患者。

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