自身免疫性脑炎
脑炎
医学
自身抗体
共济失调
免疫学
疾病
小脑共济失调
胶质纤维酸性蛋白
病理
抗体
病毒
精神科
免疫组织化学
作者
Nobuaki Yagi,Akio Kimura,Takayoshi Shimohata
出处
期刊:Brain and nerve
日期:2021-05-01
卷期号:73 (5): 631-639
标识
DOI:10.11477/mf.1416201807
摘要
Various neurological syndromes are associated with autoimmune encephalitis. Anti-mGluR1 antibody encephalitis presents mainly as subacute cerebellar ataxia, while behavioral changes and involuntary movements also occur. Anti-IgLON5 disease presents mainly as a sleep disorder. It is sometimes difficult to distinguish these diseases from other neurodegenerative diseases. Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy is seen in meningoencephalomyelitis of unknown origin. Because these new autoimmune encephalitis diseases might be treatable, early diagnosis and treatment are necessary and important to improving the condition of patients with these diseases.
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