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Characterization of neuromyelitis optica and neuromyelitis optica spectrum disorder patients with a late onset.

Authors :
Collongues, N
Marignier, R
Jacob, A
Leite, MI
Siva, A
Paul, F
Zephir, H
Akman-Demir, G
Elsone, L
Jarius, S
Papeix, C
Mutch, K
Saip, S
Wildemann, B
Kitley, J
Karabudak, R
Aktas, O
Kuscu, D
Altintas, A
Palace, J
Source :
Multiple Sclerosis Journal; Jul2014, Vol. 20 Issue 8, p1086-1094, 9p
Publication Year :
2014

Abstract

The article characterizes late onset of neuromyelitis optica (LONMO) and late onset of neuromyelitis optica spectrum disease (LONMOSD) and examines their predictive factors of disability and death. Both LONMO and LONMOSD are defined by an optic neuritis/longitudinally extensive transverse myelitis with aquaporin-4 antibodies (AQP4-Ab).

Details

Language :
English
ISSN :
13524585
Volume :
20
Issue :
8
Database :
Complementary Index
Journal :
Multiple Sclerosis Journal
Publication Type :
Academic Journal
Accession number :
97161356
Full Text :
https://doi.org/10.1177/1352458513515085