MOG antibody–associated encephalomyelitis/encephalitis

Sara Salama, Majid Khan, Santiago Pardo, Izlem Izbudak, Michael Levy

Research output: Contribution to journalReview articlepeer-review

Abstract

Myelin oligodendrocyte glycoprotein (MOG) antibody disease is a rare autoimmune disorder with antibodies against the MOG predominantly involving the optic nerve and spinal cord leading to vision loss and paralysis. When MOG antibody disease involves the brain, the phenotype is similar to acute disseminated encephalomyelitis (ADEM). In this review, we discuss MOG-positive cases presenting with encephalitis, encephalopathy, or ADEM-like presentation based on recently published series.

Original languageEnglish (US)
Pages (from-to)1427-1433
Number of pages7
JournalMultiple Sclerosis Journal
Volume25
Issue number11
DOIs
StatePublished - Oct 1 2019

Keywords

  • MOG antibody disease
  • MOG encephalomyelitis
  • MOG-EM
  • anti-MOG
  • myelin oligodendrocyte glycoprotein
  • optic neuritis
  • transverse myelitis

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

Fingerprint Dive into the research topics of 'MOG antibody–associated encephalomyelitis/encephalitis'. Together they form a unique fingerprint.

Cite this