Myopathies include a broad range of disorders. Diagnostic steps in muscle disorders should therefore be followed sequentially, in order not to miss important information and to avoid unnecessary and cost intensive diagnostic procedures. Specific care should be applied in taking patient's history to ascertain myopathy related complaints, triggers and concomitant diseases possibly being accompanied by a myopathy. Clinical examination may reveal a distribution pattern already suggestive for a specific disorder. An elevated creatin kinase, often leading to neurological evaluation, should at least be repeated once after resting. Metabolic myopathies might be detected by exercise testing. Electromyography, muscle imaging and, usually as the last diagnostic step, muscle biopsy represent further diagnostic tools in the assessment of myopathies. In some disorders molecular genetic techniques can be applied.
机构:
CHU Raymond Poincare UVSQ, AP HP, Neuromuscular Unit, Dept Pediat Neurol & Intens Cares, Garches, FranceOttawa Hosp, Neuromuscular Ctr, Ottawa, ON, Canada
Quijano-Roy, Susana
Straub, Volker
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机构:
Newcastle Univ, John Walton Muscular Dystrophy Res Ctr, Inst Genet Med, Newcastle Upon Tyne, Tyne & Wear, EnglandOttawa Hosp, Neuromuscular Ctr, Ottawa, ON, Canada
Straub, Volker
Carlier, Robert Y.
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Hop Paris, Hop Raymond Poincare, AP HP, Robert Yves Cartier Serv Radiol & Imagerie Med, Garches, France
Ctr Reference Malad Neuromusculaires Paris Nord E, Filenemus, FranceOttawa Hosp, Neuromuscular Ctr, Ottawa, ON, Canada