Abstract
Ninety-six patients with ocular myasthenia gravis (OMG) seen at Siriraj Hospital during 1994 to 2004 were retrospectively reviewed. There were 59 female (61.5%) and 37 (38.5%) male patients with mean ages of 39.5 and 33.8 years, respectively. Patients presented with initial symptoms of only ptosis in 46.9%, only diplopia in 13.5% and both ptosis and diplopia in 39.6%. However, diplopia alone is uncommon in childhood OMG. Fifteen percent developed systemic symptoms within two years of diagnosis. Thyroid function test was abnormal in 27.5% of investigated patients. Most abnormalities were hyperthyroidism. Thymoma associated with OMG is a rare condition. Most purely OMG patients can control the disease by pyridostigmine, prednisolone or immunosuppressive drugs.
| Original language | English |
|---|---|
| Pages (from-to) | 1117-1121 |
| Number of pages | 5 |
| Journal | Journal of the Medical Association of Thailand |
| Volume | 94 |
| Issue number | 9 |
| Publication status | Published - Sept 2011 |
Keywords
- Diplopia
- Generalized myasthenia gravis
- Ocular myasthenia gravis
- Ptosis
- Pyridostigmine
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