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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Detalles Bibliográficos
Autores principales: Kaga, Mihiro, Ueda, Takeshi, Yoshikawa, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10589841/
https://www.ncbi.nlm.nih.gov/pubmed/37867900
http://dx.doi.org/10.1016/j.heliyon.2023.e20912

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10589841/
https://www.ncbi.nlm.nih.gov/pubmed/37867900
http://dx.doi.org/10.1016/j.heliyon.2023.e20912

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