Pediatric glial fibrillary acidic protein meningoencephalomyelitis: A case report and review of the literature.

Mult Scler Relat Disord

Department of Pediatric Neurology, Pediatric Multiple Sclerosis Center, University of California, San Francisco Benioff Children's Hospital. 550 16th St, 4th floor, Box 0137, San Francisco, CA 94143.

Published: April 2019

A novel autoantibody, glial fibrillary acidic protein (GFAP)-IgG, has recently been associated with cases of meningoencephalomyelitis. This entity is still being unraveled. Very few pediatric patients have been identified; thus, the clinical, biological and imaging phenotype remains to be defined. Herein we describe the clinical course of a 6-year-old patient initially suspected to have a demyelinating disease but ultimately diagnosed with GFAP-IgG positive autoimmune meningoencephalomyelitis. We also provide a review of the literature regarding this novel entity.

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Source
http://dx.doi.org/10.1016/j.msard.2018.12.008DOI Listing

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