Autoimmune glial fibrillary acidic protein astrocytopathy with lesions distributed predominantly in the entire spinal cord

Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy has been considered a novel central nervous system autoimmune disease characterized by relapse and responsiveness to corticosteroid with a specific GFAP-Immunoglobulin G (IgG) being noted in cerebrospinal fluid. We report the case of a...

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Detalles Bibliográficos
Autores principales: Li, Xue-Lin, Han, Jinming, Zhao, Hao-Tian, Long, You-Ming, Zhang, Bing-Wei, Wang, Hai-Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7270931/
https://www.ncbi.nlm.nih.gov/pubmed/32547640
http://dx.doi.org/10.1177/1756286420909973

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7270931/
https://www.ncbi.nlm.nih.gov/pubmed/32547640
http://dx.doi.org/10.1177/1756286420909973

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