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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]