| Literature DB >> 15968305 |
Abstract
The combination of optic neuritis and myelitis, the so-called Neuromyelitis optica is an uncommon pattern of demyelinating disorder. In 1870, Sir Thomas Clifford Allbutt first reported the association and Erb published a comparable report. Gowers and Dreschfeld described other instances in the 19th century. This paper attempts to review the syndrome to consider whether it merits recognition as a disease, sui generis, or rather as a syndrome symptomatic of multiple sclerosis, acute disseminated encephalomyelitis, and other immunological disorders. Two forms are distinguished: a monophasic illness, and a relapsing form. The claimed differential features separating it from classical multiple sclerosis are appraised. Modern immunology suggests an antibody-dependent, complement-mediated pathogenesis. Spinal Cord (2005) 43, 631-634. doi:10.1038/sj.sc.3101758; published online 14 June 2005.Entities:
Mesh:
Year: 2005 PMID: 15968305 DOI: 10.1038/sj.sc.3101758
Source DB: PubMed Journal: Spinal Cord ISSN: 1362-4393 Impact factor: 2.772