COVID-19 and MOG-IgG-associated acquired demyelinating polyneuropathy compatible with chronic inflammatory demyelinating polyneuropathy in a previously healthy girl.
Acquired neuropathy
COVID-19
Guillain-Barré syndrome
MOG-IgG antibody
SARS-CoV2
acute disseminating encephalomyelitis
chronic inflammatory demyelinating polyneuropathy
Journal
Proceedings (Baylor University. Medical Center)
ISSN: 0899-8280
Titre abrégé: Proc (Bayl Univ Med Cent)
Pays: United States
ID NLM: 9302033
Informations de publication
Date de publication:
2022
2022
Historique:
entrez:
22
8
2022
pubmed:
23
8
2022
medline:
23
8
2022
Statut:
epublish
Résumé
Neurological manifestations of COVID-19 in the pediatric population are not as well described as those in the adult population. We describe a case of myelin oligodendrocyte glycoprotein immunoglobulin G (MOG-IgG)-associated disorder in a 9-year-old girl, who experienced complete recovery. This rare disorder is a demyelinating disease that often relapses and has the potential to cause severe morbidity. The case highlights the need for early recognition of asymptomatic and subacute presentations of demyelinating disorders and testing for MOG-IgG antibodies, as the management of presumed monophasic demyelinating disorders vs MOG-IgG-positive demyelinating disorder is different.
Identifiants
pubmed: 35991736
doi: 10.1080/08998280.2022.2088466
pii: 2088466
pmc: PMC9373784
doi:
Types de publication
Case Reports
Langues
eng
Pagination
719-721Informations de copyright
Copyright © 2022 Baylor University Medical Center.
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