A case of unusual presentation with anti-glycine receptor (GlyR) and myelin oligodentrocyte glycoprotein (MOG) antibody.
Anti-Glycine receptor antibodies
Anti-MOG antibodies
Autoimmune encephalitis
Dystonia
Myoclonus
Parkinsonism
Journal
Clinical parkinsonism & related disorders
ISSN: 2590-1125
Titre abrégé: Clin Park Relat Disord
Pays: England
ID NLM: 101761473
Informations de publication
Date de publication:
2023
2023
Historique:
received:
10
09
2022
revised:
15
02
2023
accepted:
26
03
2023
medline:
24
4
2023
pubmed:
24
4
2023
entrez:
24
04
2023
Statut:
epublish
Résumé
Movement disorders can be a prominent feature in autoimmune encephalitis. Here we present a rare case of a 73-year-old woman, who presented with a complex phenotype with encephalopathy, parkinsonism, cervical dystonia, left-sided hemidystonia and hemifacial spasm of subacute onset and was found to have breast cancer and positive anti-Glycine Receptor (GlyR) and Myelin Oligodentrocyte Glycoprotein (MOG) antibodies.
Identifiants
pubmed: 37091118
doi: 10.1016/j.prdoa.2023.100195
pii: S2590-1125(23)00013-0
pmc: PMC10119963
doi:
Types de publication
Journal Article
Langues
eng
Pagination
100195Informations de copyright
© 2023 The Author(s).
Déclaration de conflit d'intérêts
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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