Neuromyotonia, peripheral neuropathy and myasthenia gravis.
作者信息
Martinelli P, Patuelli A, Minardi C, Cau A, Riviera A M, Dal Pozzo F
机构信息
Institute of Neurology, University of Bologna, Bologna, Italy.
出版信息
Muscle Nerve. 1996 Apr;19(4):505-10. doi: 10.1002/(SICI)1097-4598(199604)19:4<505::AID-MUS10>3.0.CO;2-O.
Abstract
A patient with neuromyotonia, peripheral neuropathy and myasthenia gravis (MG) is described. Neurophysiological studies, at rest, showed continuous muscle discharges of motor unit action potentials (MUAPs) in duplets and triplets. Motor (MNCV) and sensory (SNCV) nerve conduction studies revealed mild axonal and demyelinating peripheral neuropathy. Plasma exchange was followed by disappearance of clinical and electrophysiological signs of neuromyotonia and MG, as well as peripheral neuropathy.
摘要
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