Ocular flutter as presenting manifestation of pediatric MOG antibody-associated demyelination: A case report.
MOG antibodies
MOG antibody–associated demyelination
Ocular flutter
multiple sclerosis
oscillopsia
pediatric MS
Journal
Multiple sclerosis (Houndmills, Basingstoke, England)
ISSN: 1477-0970
Titre abrégé: Mult Scler
Pays: England
ID NLM: 9509185
Informations de publication
Date de publication:
01 2019
01 2019
Historique:
pubmed:
1
11
2018
medline:
16
1
2020
entrez:
1
11
2018
Statut:
ppublish
Résumé
A 13-year-old girl presented with a 5-day history of oscillopsia. On examination, ocular flutter and mild cerebellar signs were found. Brain magnetic resonance imaging (MRI) revealed four periventricular and subcortical non-enhancing lesions. Cerebrospinal fluid (CSF) oligoclonal bands were negative. Neuroblastoma or other malignancies were not found. She responded well to a corticosteroid-intravenous immunoglobulin (IVIG) combination and remained symptom-free for 3 years until presenting again with isolated ocular flutter. Brain MRI at this time remained atypical for classic multiple sclerosis (MS) with a predominance of juxtacortical demyelinating lesions. CSF was positive for oligoclonal bands. Serum myelin oligodendrocyte glycoprotein (MOG) antibodies were present. Ocular flutter can be the presenting feature of MOG antibody-associated pediatric demyelination.
Identifiants
pubmed: 30379114
doi: 10.1177/1352458518771872
doi:
Substances chimiques
MOG protein, human
0
Myelin-Oligodendrocyte Glycoprotein
0
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
122-125Commentaires et corrections
Type : CommentIn