Neuromyelitis optica (NMO), also known as Devic syndrome, is defined clinically by severe inflammatory lesions in the optic nerves and spinal cord. Though it was lumped with multiple sclerosis for many years, it is now a clearly defined disease entity by clinical, imaging, and laboratory criteria. The main laboratory markers are high levels of antibodies to aquaporin 4, which is localized in the most affected areas. This disease may be the first of many to be separated out of the group of multiple sclerosis syndromes.
Original languageEnglish
Title of host publicationAutoimmune Disease Diagnosis: Systemic and Organ-specific Diseases, Second Edition
Subtitle of host publicationSystemic and Organ-specific Diseases
PublisherSpringer Nature
Pages583-586
Number of pages4
ISBN (Print)9783031698958
DOIs
StatePublished - Jan 2025

    Research areas

  • Aquaporin 4, Devic syndrome, Multiple sclerosis, Neuromyelitis optica

ID: 136062050