Yet Another Variant Of Gbs With Hyperrelexia And Loss Of Pain

H. Bhatia, M. Velumurugan, Ali al Bashpshe
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Abstract

Guillain Barre Syndrome is an acute demyelinating disorder of spinal roots and peripheralnerves occasionally the cranial nerves due to an immune-mediated disturbance involving the peripheral myelin sheath. It is characterized clinically by acute ascending type of motor weakness of limbs with hypoor a reflexia with preserved sensation and autonomic nervous system. However, other GBS variants like pure acute panautonomia3, Miller Fisher syndrome4, polyneuritis cranialis, pharyngeal-cervical-brachial variant5, facial diplegia with hyper reflexes6 have also been reported. Patient presented with sub acute , progressive, weakness of all four limbsassociated with hyper reflexia and loss of pain and temperature, with electrophysiological features suggestive of severe demyelinating neuropathy motor as well as sensory component and responding to IVIG.
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另一种伴有过度放松和疼痛丧失的Gbs
格林-巴利综合征是一种脊髓根和外周神经的急性脱髓鞘疾病,有时由于免疫介导的干扰累及外周髓鞘而累及脑神经。临床表现为急性上升型肢体运动性无力伴反射性亢进,感觉和自主神经系统保留。然而,其他GBS变体,如纯急性全自主神经综合征、Miller Fisher综合征、颅多神经炎、咽部-颈部-肱部变异5、面部双瘫伴反射亢进6也有报道。患者表现为亚急性、进行性、四肢无力,伴有反射亢进、疼痛和体温下降,电生理特征提示严重脱髓鞘神经病变,运动和感觉成分,对IVIG有反应。
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