Masticatory muscle strength was quantified in patients with bulbar myasthen
ia gravis and compared with that of patients with ocular myasthenia gravis,
patients in clinical remission (whether or not pharmacological) who previo
usly suffered from bulbar myasthenia gravis, and healthy subjects. Maximal
bite force and maximal activity of the masseter and temporalis muscles and
of the submental muscle complex were measured. Bite force was decreased in
the patients with bulbar myasthenia gravis, but was normal in the patients
in the clinical remission group and in the ocular group. These findings wer
e consistent with the results of electromyographic data. Although subjectiv
e reports of masticatory muscle weakness provide valuable information, quan
titative measurements provide more information about the degree of muscle w
eakness of individual muscles. This is especially important for longitudina
l evaluation of therapy in individual patients and for pharmacotherapeutic
research. (C) 2000 John Wiley & Sons, Inc.