Klin Monbl Augenheilkd 2024; 241(04): 551-553
DOI: 10.1055/a-2218-8352
Der interessante Fall

A Difficult Case of Optic Neuropathy: Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD)

Ein schwieriger Fall optischer Neuropathie: Myelin-Oligodendrozyten-Glykoprotein-Antikörper-assoziierte Erkrankung (MOGAD)

Authors

  • Celine Noha Haeller

    1   Ophthalmology, HFR, Fribourg, Switzerland
  • Thierry Badoux

    2   Neurology, HFR, Fribourg, Switzerland
  • Friedrich Medlin

    2   Neurology, HFR, Fribourg, Switzerland
  • Lionel Arlettaz

    3   Allergology and Clinical Immunology, Hôpital du Valais, Sion, Switzerland
  • Philippe DeGottrau

    1   Ophthalmology, HFR, Fribourg, Switzerland
  • Eva Grams

    1   Ophthalmology, HFR, Fribourg, Switzerland
  • Manolito Lucas Finger

    1   Ophthalmology, HFR, Fribourg, Switzerland
  • Vincent Dunet

    4   Medical Radiology, CHUV, Lausanne, Switzerland
  • Marie-Claire Gaillard

    1   Ophthalmology, HFR, Fribourg, Switzerland
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Background

Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is a recently defined inflammatory demyelinating disease, that generally affects the optic nerve (ON) in adults and the central nervous system in children [1], [2]. The specific clinical phenotype, radiological findings, and neurological manifestations enable its distinction from other central nervous system inflammatory demyelinating diseases (CNS IDDs) such as aquaporine-4-IgGQ neuromyelitis optica spectrum disorder (NMOSD) and multiple sclerosis (MS) [3] [4] [5].



Publication History

Received: 27 October 2023

Accepted: 27 November 2023

Article published online:
23 April 2024

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