A Clinician's View of Neuromuscular Diseases |
Contents
Chapter 5 MUSCULAR DYSTROPHIES | 95 |
Chapter 6 MYOTONIA | 125 |
Chapter 7 INFLAMMATORY MYOPATHIES | 138 |
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abnormal acid activity acute appearance Arch arms associated attack become begins body carriers cause cells changes characteristic child clinical common creatine decreased deficiency demonstrate described detected develop diagnosis difficulty Duchenne's early effect elevation Engel enzyme evaluation evidence examination exercise fasciculations fibers Figure findings foot frequently function give glucose groups hand helpful illness increased inherited involved knee known Laboratory later legs less levels limb medication membrane mild motor neuron disease movement muscle biopsy muscle fibers muscular dystrophy myasthenia gravis myopathy myotonia nerve neuromuscular neuropathy normal noted noticed occur pain paralysis particularly patients perhaps period peripheral polymyositis position possible potentials present probably produced progressive proximal rare reported respiratory response rest seems seen serum severe shoulder showed side signs similar spinal muscular atrophy strength studies suggested symptoms syndrome treatment Type usually variety walk wasting weakness