| Literature DB >> 30885369 |
Carla Francisco1, Katherine Meddles2, Emmanuelle Waubant3.
Abstract
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. Published by Elsevier B.V.Entities:
Keywords: Case report; GFAP; Glial fibrillary acidic protein; Meningoencephalomyelitis; Pediatric
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Year: 2018 PMID: 30885369 DOI: 10.1016/j.msard.2018.12.008
Source DB: PubMed Journal: Mult Scler Relat Disord ISSN: 2211-0348 Impact factor: 4.339