1.
Chinese Journal of Neurology
;
(12): 82-87, 2023.
Artigo
em Chinês
| WPRIM
| ID: wpr-994803
RESUMO
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.