| Literature DB >> 32474284 |
Yue Zhang1, Abhijeet Kumar Bhekharee2, Xiang Zhang3.
Abstract
We describe a 43-year-old female whose manifestations fulfilled the diagnostic criteria of aquaporin-4 IgG negative neuromyelitis optica spectrum disorders (NMOSD). High titer of glial fibrillary acidic protein (GFAP) antibody was detected in cerebrospinal fluid. In this case, some symptoms pertained to NMOSD and some to GFAP antibody-related disorders. The patient had a good response to corticosteroids.Entities:
Keywords: Aquaporin-4 IgG negative neuromyelitis optica spectrum disorders; Glial fibrillary acidic protein antibody
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Year: 2020 PMID： 32474284 DOI： 10.1016/j.msard.2020.102202
Source DB: PubMed Journal: Mult Scler Relat Disord ISSN： 2211-0348 Impact factor: 4.339