Three cases of ocular myasthenia gravis were observed. The first patie
nt, a 74-year-old man was found to have complete left ophthalmoplegia
and ptosis unchanged at examination one month after onset. The second
patient, a 42-year-old man, developed incomplete right ophthalmoplegia
with peudoanterior internuclearis ophthalmoplegia, then ptosis two da
ys later. The third patient, a 70-year-old man, presented with sudden
onset complete right palsy of the third nerve. Diabetes mellitus or in
tra-cranial lesions were suspected in all three patients although labo
ratory tests, tomodensitometry, nuclear magnetic resonance imaging, or
arteriography gave no confirmation. Ptosis was relieved and eye movem
ent was improved after the intravenous edrophonium test, but electromy
ography was negative. The three patients were treated with anticholine
sterase agents and showed unequivocal improvement. The second patient
underwent thymectomy. Clinicians should inform patients of the contrai
ndications of drugs in this disease. The diagnosis of pure oculomotor
forms of myasthenia gravis is sometimes difficult to establish and sho
uld be suspected in cases of unexplained oculomotor palsy.