[On the clinical aspects and pathogenesis of neuromuscular diseases].
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Biomedical subjects
Publications and source records attributed to B M Gekht.
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For many years myasthenia was classed among the rare neurological diseases. At the present time, because of an improvement in diagnosis and, possibly also because this disease has become widespread, the number of cases recorded has appreciably increased and comprises more than 3 per 100,000 population [1, 2]. More than 200 myasthenia patients are under our observation. From 2 to 10 patients come under observation annually.
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The paper deals with the studies of the distribution pattern of various clinical manifestations of demyelinated polyneuropathies made in 211 patients during 9 years. An electromyographic study was performed by using the apparatuses made in Russia. The clinical diagnostic criteria evidenced by electromyography (EMG) enable the authors to formulate the specific features of algorithms of data processing and to develop a special software that expands the potentialities of up-to-date EMG apparatuses.
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