We conducted a multicenter retrospective study in a cohort of pediatric patients (age <18) with seropositive MOGAD. Patient’s demographics and clinical management information were extracted from electronic medical record system. Retinal nerve fiber layer (RNFL) thickness and median deviation (MD) were collected via neuro-ophthalmic testing.
Eighteen patients were included in the study with a median age of onset 10 years (6-14), 12/18 were female, 6/18 were male, 13/18 (72%) presented with isolated ON as the first event, remaining five patients had ON as a part of combined demyelinating phenotype at the first event. Median follow-up was 31 months (5-41). 3/18 (17%) had recurrent ON alone, 3/18 (17%) relapsed with other phenotypes (TM, cerebellar attack, encephalitis, ADEM); six patients (28%) had bilateral optic nerve involvement during initial attack. Mean LogMAR visual acuity was 1.7 at onset in 24 affected eyes. Maximum visual recovery to LogMAR 0 is attained in 1 month (1-1.5) in 16 eyes. Median RNFL thickness within two weeks of ON onset is 180 microns (IQR: 146-250) in seven eyes without correlation to log MAR outcomes at two weeks with median 0.6 (IQR:0.2 to 2, P=0.16) or at two months with median 0 (IQR: 0-0.1, P=0.2)
Pediatric patients with MOGAD related optic neuritis often return to baseline visual acuity.