{"title":"诊断急性球麻痹加综合征：格林-巴利综合征的罕见变种","authors":"Stuti Sharma, Neha Rajpal","doi":"10.9734/jpri/2024/v36i47511","DOIUrl":null,"url":null,"abstract":"Presenting case of a 11-year-old girl with sudden cranial nerve weakness, universal areflexia but without limb pain or weakness. NCV showed subclinical axonal involvement in limbs. A diagnosis of acute bulbar palsy plus–GBS was made and child was started on Iv Immunoglobulins which showed significant improvement. This report is for raising awareness about this variant of GBS.","PeriodicalId":506675,"journal":{"name":"Journal of Pharmaceutical Research International","volume":"6 4","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Diagnosis of Acute Bulbar Palsy Plus Syndrome: A Rare Variant of Guillain–barre Syndrome\",\"authors\":\"Stuti Sharma, Neha Rajpal\",\"doi\":\"10.9734/jpri/2024/v36i47511\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Presenting case of a 11-year-old girl with sudden cranial nerve weakness, universal areflexia but without limb pain or weakness. NCV showed subclinical axonal involvement in limbs. A diagnosis of acute bulbar palsy plus–GBS was made and child was started on Iv Immunoglobulins which showed significant improvement. This report is for raising awareness about this variant of GBS.\",\"PeriodicalId\":506675,\"journal\":{\"name\":\"Journal of Pharmaceutical Research International\",\"volume\":\"6 4\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-04-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Pharmaceutical Research International\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.9734/jpri/2024/v36i47511\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pharmaceutical Research International","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9734/jpri/2024/v36i47511","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
这是一个 11 岁女孩的病例，她患有突发性颅神经无力和普遍性反射障碍，但没有肢体疼痛或无力。NCV显示四肢亚临床轴索受累。诊断结果为急性球麻痹+GBS，患儿开始服用 Iv 免疫球蛋白，病情明显好转。本报告旨在提高人们对这种变异型 GBS 的认识。
Diagnosis of Acute Bulbar Palsy Plus Syndrome: A Rare Variant of Guillain–barre Syndrome
Presenting case of a 11-year-old girl with sudden cranial nerve weakness, universal areflexia but without limb pain or weakness. NCV showed subclinical axonal involvement in limbs. A diagnosis of acute bulbar palsy plus–GBS was made and child was started on Iv Immunoglobulins which showed significant improvement. This report is for raising awareness about this variant of GBS.
求助内容：
应助结果提醒方式：
京公网安备 11010802042870号
