医学
病因学
共济失调
脑炎
格林-巴利综合征
儿科
外眼肌麻痹
米勒-费希尔综合征
神经学
疾病
重症监护医学
病理
免疫学
精神科
病毒
化学
基因
生物化学
线粒体DNA
作者
Muhammad Haisum Maqsood,Kinza Rubab,Muhammad Maqsood
出处
期刊:The professional medical journal
[Independent Medical Trust]
日期:2019-08-02
卷期号:26 (08): 1386-1388
被引量:1
标识
DOI:10.29309/tpmj/2019.26.08.3135
摘要
Bickerstaff’s brainstem encephalitis (BBE) is a rare neurological disease characterized by ophthalmoplegia, ataxia and altered sensorium.1 Its etiology is thought to be autoimmune in nature and sometimes certain infections precede illness.2-4 It is a spectrum of illnesses with Guillain-Barre Syndrome (GBS) and Miller Fischer Syndrome (MFS).5-6 We describe an atypical case of BBE which was initially misdiagnosed as meningo-encephalitis. As such, we report this case for its rarity. Informed consent was received from the patient before undertaking and reporting this study.
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