首页> 外文期刊>Journal of clinical neuromuscular disease >Acute Flaccid Myelitis With Early, Severe Compound Muscle Action Potential Amplitude Reduction: A 3-Year Follow-up of a Child Patient
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Acute Flaccid Myelitis With Early, Severe Compound Muscle Action Potential Amplitude Reduction: A 3-Year Follow-up of a Child Patient

机译:急性弛缓性脊髓炎早期,严重的复合肌动作潜在幅度减少:儿童患者的3年随访

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摘要

The term "acute flaccid myelitis (АРМ)" refers to cases of acute flaccid weakness with spinal cord gray matter lesions on magnetic resonance imaging (MRI) or evidence of spinal cord motor neuron injury on electrodiagnostic testing. We describe a long-term follow-up of an AFM child presenting with tetraparesis and marked compound muscle action potential (CMAP) attenuation.A 3-year-old boy was admitted with a 4-day history of drowsiness, motor hypo-activity, and areflexia, requiring mechanical ventilation for 8 weeks. On follow-up over 3 years, there has been some degree of improvement of muscle power, although the patient is chairbound with generalized amyotrophy and areflexia.
机译:术语“急性弛缓性骨髓炎(Арм)”是指在磁共振成像(MRI)上具有脊髓灰质病变的急性松弛弱症的病例或脊髓电机神经元损伤对电渗诊检测的证据。 我们描述了一个患有Tetraparis的AFM儿童的长期随访,并标记复合肌肉作用潜力(CMAP)衰减。3岁的男孩接纳了4天的嗜睡,电机的嗜睡史, 并令人壁脂,需要机械通风8周。 在3年后跟进后,肌肉力量有一定程度的提高,尽管患者是具有广义肌肤萎缩和令人反感的障碍。

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