Comparative study of AQP4‑NMOSD, MOGAD and seronegative NMOSD: a single‑center Belgian cohort

peer reviewed ; Objectives: To emphasize physio-pathological, clinical and prognosis differences between conditions causing serious and sometimes very similar clinical manifestations: anti-aquaporin-4 (AQP4) and anti-myelin oligodendrocyte glycoprotein (MOG) antibodies related diseases, and seronegative NMOSD (neuromyelitis optica spectrum disorders). Methods: Based on diagnostic criteria for NMOSD and MOGAD (MOG associated disorders), we retrospectively surveyed 10 AQP4-NMOSD, 8 MOGAD and 2 seronegative NMOSD, followed at the specialized neuroimmunology unit of the CHU Liege. Results: Female... Mehr ...

Verfasser: Dauby, Solène
DIVE, Dominique
LUTTERI, Laurence
ANDRIS, Cécile
HANSEN, Isabelle
MAQUET, Pierre
LOMMERS, Emilie
Dokumenttyp: journal article
Erscheinungsdatum: 2022
Verlag/Hrsg.: Acta Medica Belgica
Schlagwörter: Neuromyelitis optica / MOG-associated disorders / QP4-antibody NMO spectrum disorders / Human health sciences / Neurology / Sciences de la santé humaine / Neurologie
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26535207
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://orbi.uliege.be/handle/2268/262215