In a retrospective review, the eye symptoms of 17 children (mean age:
13 1/2 years) who had definite multiple sclerosis (Poser's criteria) a
nd 15 who had probable multiple sclerosis over the last 18 years were
evaluated, Follow-up varied from 3 weeks-to 6 years. Of 94% of childre
n (16 of 17) with ophthalmologic symptoms, 47% (8 of 17) presented wit
h an initial disturbance of vision, Twelve children had optic neuritis
, 1 progressive uveitis, and 4 brainstem symptoms (i,e,, VIth nerve pa
lsy, 1 1/2 syndrome, internuclear ophthalmoplegia), Four children had
cerebellar signs (nystagmus, saccadic pursuit), In 4 children, clinica
l localization was less specific, Recovery was generally good in most
of the children; cerebellar problems were most persistent, Multimodal
potentials were more helpful for investigation of optic neuritis and c
erebellar lesions than for brainstem lesions, In the cohort of probabl
e multiple sclerosis of 15 children, 11 had eye symptoms (5 with neuro
myelitis optica, 4 optic neuritis, 1 internuclear ophthalmoplegia, and
1 cerebellar symptoms), Ophthalmologic symptoms are slightly more fre
quent in children with multiple sclerosis than in adults and should be
specifically investigated to establish the diagnosis.