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Table 1 Patient numbers and diagnoses

From: MOG-IgG in NMO and related disorders: a multicenter study of 50 patients. Part 2: Epidemiology, clinical presentation, radiological and laboratory features, treatment responses, and long-term outcome

Diagnostic categories N (%)
History of ON and/or MY 50/50 (100%)
History of ON 44/50 (88%)
History of myelitis 28/50 (56%)
Meeting Wingerchuk’s 2006 criteria for NMOa 14/50 (28%)
Meeting 2015 consensus criteria for NMOSDb 16/50 (32%)
Meeting 2010 McDonald criteria for MSc 15/46 (33%)
History of ON and of myelitis 22/50 (44%)
Meeting Wingerchuk’s 2006 criteria for NMOa 14/22 (63.6%)
Meeting 2015 consensus criteria for NMOSDb 15/22 (68.2%)
History of ON but not of myelitis 22 (44%)
Meeting Wingerchuk’s 2006 criteria for NMOa 0/22 (0%)
Meeting 2015 consensus criteria for NMOSDb 1/22 (4.5%)
History of myelitis but not of ON 6/50 (12%)
Meeting Wingerchuk’s 2006 criteria for NMOa 0/6 (0%)
Meeting 2015 consensus criteria for NMOSDb 0/6 (0%)
  1. MS multiple sclerosis, NMO neuromyelitis optica, NMOSD NMO spectrum disorder, ON optic neuritis. asee ref. [28], bsee ref. [29], csee ref. [46]