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Items in the history and physical examination along with results of certain simple tests performed in the office (ice test, sleep test, and edrophonium test) are useful in predicting the likelihood of myasthenia gravis. These results must be interpreted with caution, however, given the high prevalence of disease in the populations reported in clinical studies. This review is limited by the small number of signs and symptoms scientifically studied and reported in the literature. Future studies evaluating the value of common historical features and easy maneuvers commonly known and practiced by experts in the clinical diagnosis of myasthenia are needed. |
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acetylcholine receptor antibody
diplopia
diplopia,transient
dysarthria
dysphagia
dysphonia
electromyogram,decremental response
myasthenia gravis
myasthenia gravis,cold test for
myasthenia gravis,diagnosis
myasthenia gravis,neuromuscular junction in
myasthenia gravis,receptor site in
nasal speech
nerve conduction studies
neurologic disease,diagnoses of
neurologic examination
neurologic history
neurologic signs
neurologic symptoms
neuromuscular disease,electrodiagnosis of
neuromuscular junction
neuromuscular junction,abnormality of
peek sign
ptosis
ptosis,unilateral
repetitive nerve stimulation
review article
sleep
tensilon test
weakness,end of day
weakness,fatiguable
weakness,generalized
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