医学
代谢型谷氨酸受体1
小脑共济失调
共济失调
代谢型谷氨酸受体
眼球震颤
嗜睡症
神经科学
谷氨酸受体
内科学
病理
听力学
心理学
受体
神经学
精神科
作者
LiTing Goh,Furene Sijia Wang,Velda X. Han,J. Lin
出处
期刊:Neurology
[Ovid Technologies (Wolters Kluwer)]
日期:2022-11-08
卷期号:99 (19): 862-863
被引量:2
标识
DOI:10.1212/wnl.0000000000201268
摘要
A 15-year-old boy developed progressive cerebellar dysfunction over 3 weeks. Examination showed ataxic gait, unsteady tandem gait, horizontal nystagmus, intention tremor, and ataxia on heel-toe-shin testing (Video 1, [links.lww.com/WNL/C323][1]). Dysdiadochokinesia and dysarthria were found but not illustrated in the video. Neuroimaging and CSF biochemistry was normal. Serum and CSF metabotropic glutamate receptor type 1 (anti-mGluR1) autoantibodies were found. His cerebellar function improved markedly within 3 months of initiating immunotherapy (Video 1, [links.lww.com/WNL/C323][1]). The median age at onset of anti-mGluR1 encephalitis is 55 years.1,2 Paraneoplastic syndromes should be considered, but anti-mGluR1 encephalitis is more often autoimmune in younger patients.1,2 [1]: http://links.lww.com/WNL/C323
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