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Other causes of megaesophagus include myasthenia gravis, lead poisoning, and Addison's disease.

其他疾病也可引发巨食道症,如重症肌无力、铅中毒和艾迪生氏病。

Hirayama disease should be considered for young patient,especially male patient,with asymmetrical amyasthenia and amyotrophy in the hand and forearm.Hirayama disease can be diagnosed if MR abnormalities of the lower cervical dural sac and spinal cord are seen in a fully flexed position.

当遇到青少年出现手及前臂不对称的肌无力和萎缩而无感觉障碍时,应首先考虑有平山病的可能,可进一步行屈颈MR检查,出现下颈髓及其硬膜囊的特征性表现可确诊。

Other disfluencies are associated with neuropathology such as the speech characteristics associated with apraxia, parkinsonism, multiple sclerosis, myasthenia gravis and others.

其他的非流畅语言表达都会涉及到神经病理学,比如由功能丧失症、帕金森病、多发性硬化症、重症肌无力和其他类似疾病所导致不流畅语言表达。

Methods 16 patients who were diagnosed as myasthenia gravis with initial head and neck symptoms were determined by a pure tone audiometer and acoustic immitance measurement and then the acoustic reflex was reexamined 30 min after injection of Neostigminum sulfate 0.5~1?

对以头颈部和五官症状为首发症状而到我科初诊的16例重症肌无力患者进行纯音测听和声导抗检测,并在肌肉注射甲基硫酸新斯的明0.5~1.0?mg,30?min后复查声反射。检测用0.5、1.0、2.0和4.0?kHz的纯音作同侧和对侧刺激,比较用药前后有无声反射及其阈值、振幅变化、有无衰减等。

June MG Awareness Month National Proclamation - Please Contact Your Congressperson Today!

抓紧联系当地议员,促成六月成为美国重症肌无力防治月

Results The mainly clinical features of the patients with PLS included:insidious onset,slowly progressive,four limbs amyosthenia,hypermyotonia,tendon hyperreflexia,positive pathologic reflexes and pseudobulbar palsy symptom.

结果 本组PLS患者主要临床特点为:起病隐袭、逐渐加重;四肢肌无力、肌张力增高、腱反射亢进、病理征阳性、假性延髓麻痹症状。

Abstract] Objective:To investigate extraocular muscles susceptibility to myasthenia gravis.

目的:探讨重症肌无力患者眼外肌易于受累的机制。

Fatigue,arthritis, weight losing,muscular pain,weakness of the muscle and pneumonopathy in the late-onset group were significantly higher than that in the early-onset group.

晚发组发病到确诊的平均时间长,疲乏、关节痛、体重下降、肌痛肌无力、肺部病变发生率高,肾损害、雷诺现象、脱发的发生率低(P<0.05),血沉增快、肝功能损害检出率高,而补体(C3C4)降低、白蛋白降低、dsDNA阳性检出率低(P<0.05)。

Raynauds phenomenon, arthralgia/arthritis, fever, muscle involvement, swollen hands/sclerodactyly and abnormally elevated IgG and ESR levels were seen frequently in the disease course. Morbidity of pulmonary interstitial fibrosis was 40%. Renal involvement was not found in 15 cases of MCTD patients.

首发症状主要为雷诺现象(86.7%),其次为关节痛/关节炎(13.3%);临床表现中雷诺现象、关节痛/关节炎、发热、肌无力/肌炎、手指肿胀常见,实验室指标中IgG和血沉增高发生率高,肺间质病变发生率为40%,15例MCTD均无明显肾脏受累。

Call their healthcare professional if they experience any of the following: muscle pain, tenderness or weakness, urine that is dark or red-colored, or unexplained tiredness.

8226;如果出现以下任一情况,请给自己的医生打电话:肌痛,或肌无力,尿色变深或者变红,或者不能解释的疲乏。

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