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Acute Guillain-Barré syndrome: A case report in pediatrics

机译:急性格林-巴雷综合征:儿科病例报告

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Guillain-Barré syndrome is a complicated degenerative neurological disorder which can be either acute or chronic in nature. Guillain-Barré syndrome is an acquired condition and is characterized by progressive, symmetrical, proximal and distal tingling and weakness. Muscle stretch reflexes are decreased to absent and loss of sensation is common. A 4-year female child with no significant past medical history who presented with progressive weakness involving both upper and lower limbs over 48 to 72 h and complaints of tachypnea and hypotonia involving all group of muscles was admitted in Sri Venkateswara Ramnarayan Ruia Government General Hospital, Tirupati. In the present report, the main clinical aspects and features of Guillain-Barré syndrome along with the multidisciplinary approach to the acute phase combining supportive and high dose of immunoglobulin therapy were practiced. Patient should have follow-up within 2 weeks after the acute syndrome to evaluate for relapse, at which point repeat intravenous immunoglobulin. Thereafter, follow-up is necessary for every 4–6 weeks for 6 months, then 6 months for 1 year and then yearly.
机译:格林-巴雷综合征是一种复杂的变性神经系统疾病,本质上可以是急性或慢性的。格林-巴雷综合征是一种获得性疾病,其特征是进行性,对称性,近端和远端刺痛和无力。肌肉舒展反射减少到消失,感觉丧失是常见的。 Sri Venkateswara Ramnarayan Ruia政府总医院收治了一个4岁的女性儿童,该儿童没有明显的既往病史,在48至72小时内表现出上肢和下肢渐进性无力,涉及所有肌肉群的呼吸急促和肌张力减退,蒂鲁伯蒂。在本报告中,实践了格林-巴利综合征的主要临床方面和特征,以及支持和大剂量免疫球蛋白治疗相结合的急性期的多学科方法。患者应在急性综合征后2周内进行随访以评估其复发情况,此时应重复静脉内免疫球蛋白治疗。此后,必须每4-6周进行一次随访,持续6个月,然后每6个月进行1年,然后每年一次。

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