A 52-year-old patient developed an eye movement disorder first resembling a
left internuclear ophthalmoplegia and subsequently a "one-and-a-half syndr
ome" as the presenting symptoms of ocular myasthenia gravis. No accompanyin
g myasthenic features were present except for the fluctuation in the amplit
ude of dissociated nystagmus. This patient shows that an oculomotor disorde
r considered a typical pontine lesion may instead be caused by myasthenia g
ravis, even in the absence of other clinical and electrophysiologic feature
s of neuromuscular deficit.