查询词典 nystagmus

It may also cause hypokalemia. Symptoms of low serum magnesium are muscular tremors and fasciculations, ocular nystagmus, tetany, altered mental state, and cardiac arrhythmias such as torsades de pointes (multifocal ventricular tachycardia).

低镁血症主要表现为肌肉震颤和肌束自发性收缩，眼震，手足搐搦，神志改变和心律失常，例如尖端扭转性室速。

Light from fetal distress after birth may not leave any residual disease, may moderate the impact of mental development; weight can be left over from large cerebral palsy, understanding the brain can EEG cases, B-, CT, MRI and so on. 2, it is necessary to dynamically check the basis of objective indicators to determine whether or not a normal baby brain development. 3, kept shaking his head should be excluded from the following disorders: 1, eye disorders:(1) nystagmus (2) congenital hypoplasia of extraocular muscles (3) congenital strabismus Second, epilepsy: A, wast syndrome: also known as Infantile Spasms B, lenox syndrome, also known as slow-slow-wave epileptic encephalopathy spine. C, calcium deficiency caused by muscle contraction, tetany.

胎儿宫内窘迫轻者生后可不留任何遗症，中度者可影响智力发育；重者可遗留大脑瘫、了解大脑情况可做脑电图、B超、CT、核磁共振等。2、要动态地根据客观检查的各项指标来判断孩子大脑发育正常与否。3、不停地摇头应排除以下疾患：一、眼部疾患：(1)眼球震颤(2)先天性眼外肌发育不全(3)先天性斜视二、癫痫：A、wast综合症：也称婴儿痉挛症B、lenox综合症，也称慢波慢棘癫痫性脑病。C、缺钙引起肌肉收缩，手足搐搦。

In most cases, rotation to the pathological side from supine position caused a very intense horizontal nystagmus beating towards the undermost ear.

仰卧侧头位试验可诱发水平向地性眼震，无潜伏期和疲劳性。

PURPOSE: Infantile esotropia is linked strongly to latent fixation nystagmus in human infants, but many features of this comorbidity are unknown.

目的：人类幼儿先天性内斜视与隐性注视性眼球震颤密切相关，但有关此病的很多特点还不清楚。

Sensory impairment and urinary dysfunction also had developed, and paraparesis persisted after the hypokalemia was corrected during hospitalization. An optokinetic nystagmus test showed bilateral sick waves and at the same time a cerebrospinal fluid analysis was normal. A blood examination disclosed borderline anti-nuclear antibodies and an elevated serum IgG level. Her cervical spinal cord showed mild swelling and contrast-enhancement when examined by magnetic resonance imaging. Neither a brain stem nor an optic nerve's lesion was found. Based on the above, acute transverse myelitis was diagnosed. All the symptoms present in the patient relieved gradually after 5-days of pulsed intravenous methylprednisolone therapy.

一50岁女性，因为眩晕、前额头痛、视力模糊、恶心、呕吐及两侧下肢无力而求诊，於低血钾矫正后，两侧下肢无力依然持续，并发生胸部以下感觉缺损及排尿困难等现象，视运动性眼振检查显示两侧波形障碍，脑脊液检查正常，血液学检查显示抗核酸抗体及血清IgG指数偏高，显影剂增强磁振造影显示颈段脊髓肿大且略为显影，并无脑干或视神经的病灶，诊断为急性横断性脊髓炎，给予静脉注射类固醇后症状逐渐缓解。

Besides, the numerical analysis showed that the pendular nystagmus followed with horizontal strabismus could be treated by changing the eye balance positions by adjusting the operation amounts of medial rectus and lateral rectus respectively.

此外，计算分析还表明，当钟摆型眼球震颤伴有水平斜视时，可用分别改变内外直肌的后固定量，造成使眼球的静平衡位置发生变化的办法来治疗。

Optokinetic nystagmus inducing therapy preferentially affects reading saccades in the direction of the induced saccadic component.

在诱导扫视成分的方向上，视动性眼球震颤诱导疗法优先影响阅读扫视。

ENG recorded tow kinds of nystagmus waveforms,included subsultus waveform as saw tooth wave and pendulum waveform as sinusoidal wave.

眼震电图可以记录到跳动型和钟摆型两种不同的眼震波，跳动型呈锯齿波，钟摆型呈正旋波。

The albinism is characterized by hypopigmentation of the skin and hair and the ocular findings of reduced iris pigment with iris transillumination, reduced retinal pigment, foveal hypoplasia with significant reduction in visual acuity (usually in the range of 20/50 to 20/400), nystagmus, and increased crossing of the optic nerve fibers.

白化的特征有：皮肤与头发的色素减退以及一些眼科症状，包括虹膜透照显示出的虹膜着色减弱、视网膜着色减弱、中央凹发育不良且视觉灵敏度显著减弱（通常在20/50至20/400的范围）、眼球震颤和视神经纤维交叉增加。

Diagnosis/testing. A diagnosis of ocular albinism is probable in the presence of congenital nystagmus, iris translucency, and significant hypopigmentation of the ocular fundus periphery in males with normal skin pigmentation and foveal hypoplasia, reduced visual acuity, and aberrant optic pathway projection, as demonstrated by crossed asymmetry of the cortical responses on visual evoked potential. X-linked inheritance is documented by either a family history consistent with X-linked inheritance or the presence of typical carrier signs (irregular retinal pigmentation and partial iris transillumination) in an obligate carrier female.

诊断/检测。对于皮肤色素沉着正常、中央凹发育不全、视敏度降低以及视径投射异常（VEP，表现为视觉诱发电位中皮层反应的交叉不对称）的男性患者，当存在先天眼球震颤、虹膜半透明以及显著的眼基底层边缘色素减退的症状时，可被疑似诊断为眼白化病。X连锁性遗传则以存在与X连锁遗传一致的家族病史，或在一个应当为携带者的女性中存在典型的携带者迹象（视网膜色素沉着不规则以及部分虹膜透射）而被确认。

I didn't watch TV last night, because it .

昨晚我没有看电视，因为电视机坏了。

Since this year, in a lot of villages of Beijing, TV of elevator liquid crystal was removed.

今年以来，在北京的很多小区里，电梯液晶电视被撤了下来。