A rare case of glial fibrillary acidic protein astrocytopathy that resolved spontaneously within a self-limited course

Glial fibrillary acidic protein astrocytopathy is a form of autoimmune meningoencephalomyelitis. The presence of antibodies in spinal fluid against glial fibrillary acidic protein is necessary to diagnose the disease. There is no standard treatment and few cases of glial fibrillary acidic protein as...

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Bibliographic Details
Main Authors: Mihiro Kaga, Takeshi Ueda, Satoshi Yoshikawa
Format: Article
Language:English
Published: Elsevier 2023-10-01
Series:Heliyon
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844023081203