Neuro-ophthalmologische Präsentation der Retrobulbärneuritis im Rahmen der Myelin-Oligodendrozyten-Glykoprotein-Antikörper-assoziierten Erkrankung
Ting-Yi Lin, Susanna Asseyer, Gilberto Solorza Buenrostro, Kristina Feldmann, Steffen Hamann, Friedemann Paul, Hanna Zimmermann · Klinische Monatsblätter für Augenheilkunde · 2022 · Heft 08
Bibliografische Angaben
Zusammenfassung
(English) Myelin oligodendrocyte glycoprotein antibody‐associated disease (MOGAD) is a rare demyelinating autoimmune disorder of the central nervous system. MOGAD frequently manifests with severe, bilateral, and recurrent optic neuritis (ON) episodes and is an important differential diagnosis to multiple sclerosis and aquaporin-4-IgG seropositive neuromyelitis optica spectrum disorders. The clinical manifestations of MOGAD commonly include, besides ON, transverse myelitis, acute disseminated encephalomyelitis, or brainstem encephalitis. In this article, we summarize the current knowledge of the neuro-ophthalmolo…