Autoimmune glial fibrillary acidic protein astrocytopathy
10.3760/cma.j.cn113694-20221002-00745
- VernacularTitle:自身免疫性胶质纤维酸性蛋白星形胶质细胞病
- Author:
Xiaokun QI
1
;
Dongwei DIAO
Author Information
1. 解放军总医院第六医学中心神经内科，北京 100048
- Keywords:
Glial fibrillary acidic protein;
Anti-GFAP autoantibody;
Meningoencephalitis;
Peripheral nervous system;
Treatment
- From:
Chinese Journal of Neurology
2023;56(1):82-87
- CountryChina
- Language:Chinese
-
Abstract:
Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy is a rare immune-mediated inflammatory disease of central nervous system reported in recent years, and its specific biological marker is anti-GFAP autoantibody. In this paper, the etiology, pathogenesis, clinical manifestations, auxiliary examination and treatment of the disease are comprehensively expounded, so as to improve the understanding of clinicians, especially neurologists.
