Literature DB >> 21444020

Metabolic myopathies: clinical features and diagnostic approach.

Edward C Smith1, Areeg El-Gharbawy, Dwight D Koeberl.   

Abstract

The rheumatologist is frequently called on to evaluate patients with complaints of myalgia, muscle cramps, and fatigue. The evaluation of these patients presents a diagnostic challenge given the nonspecific and intermittent nature of their complaints, often leading to inappropriate diagnostic testing. When these symptoms are associated with physical exertion, a metabolic myopathy should be suspected Although inflammatory myopathies may present with similar features, such a pattern should prompt a thorough evaluation for an underlying metabolic myopathy. This review discusses the most common causes of metabolic myopathies and reviews the current diagnostic options available to the clinician.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21444020     DOI: 10.1016/j.rdc.2011.01.004

Source DB:  PubMed          Journal:  Rheum Dis Clin North Am        ISSN: 0889-857X            Impact factor:   2.670


  1 in total

1.  Cellular prion protein dysfunction in a prototypical inherited metabolic myopathy.

Authors:  Sophie Mouillet-Richard; Fatima Djouadi; Fatima-Zohra Boufroura; Céline Tomkiewicz-Raulet; Virginie Poindessous; Johan Castille; Jean-Luc Vilotte; Jean Bastin
Journal:  Cell Mol Life Sci       Date:  2020-09-01       Impact factor: 9.261

  1 in total

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