Guillain-Barre Syndrome: Case Report

N. Mustafa, Hajra Sarwer, Muhammad Afzal, M. Arif
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引用次数: 1

Abstract

Guillain Barre Syndrome (GBS) is acute onset. It is auto immune mediated neuropathy. Nutrition play important role in GBS patients. GBS is no traumatic disorder. It is paralytic diseases in developing countries. The auto antibodies are present against the various antigens in peripheral regions. The occurrence of this disease is very rare. The incidence of the GBS is 0.4 to 1.7 per million people per year. GBS have subtypes acute motor axonal neuropathy (AMAN), and ADIP acute inflammatory demyelinating polyneuropathy. A 12 years old male patient admitted in Government hospital with the complaint of inability to walk and stand. His lower extremities become weak. He cannot stand up and he was unable to walk. After hospitalization treatment given to patient after few days he was discharged. He referred to nutritional support. A team gives him medical therapy. After labs and blood tests, the result is obtained GBS positive. A significant result obtained than it would be treated. GBS is very rare disease. The diagnosis is very difficult. In this condition the patient progressively weak their extremities. The disorder in limbs weakness increase day by day.
格林-巴利综合征1例报告
格林-巴利综合征(GBS)为急性发病。这是一种自身免疫介导的神经病。营养在GBS患者中起重要作用。GBS不是创伤性障碍。它是发展中国家的麻痹性疾病。自身抗体在外周区域针对各种抗原存在。这种病的发生很罕见。GBS的发病率为每年每百万人0.4至1.7人。GBS有急性运动轴索神经病(AMAN)和急性炎性脱髓鞘多神经病变(ADIP)亚型。一名十二岁男病人因不能行走及站立而入住政府医院。他的下肢变得虚弱。他不能站起来,也不能走路。病人住院治疗几天后出院。他提到了营养支持。一个小组给他进行药物治疗。经化验及血液检查,结果为GBS阳性。得到了比处理结果更重要的结果。GBS是一种非常罕见的疾病。诊断非常困难。在这种情况下,病人的四肢逐渐衰弱。四肢无力的病症日益增多。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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