Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/63299
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Type: Journal article
Title: Idiopathic inflammatory myopathies: diagnostic criteria, classification and epidemiological features
Author: Cox, S.
Limaye, V.
Hill, C.
Blumbergs, P.
Roberts-Thomson, P.
Citation: International Journal of Rheumatic Diseases, 2010; 13(2):117-124
Publisher: Wiley-Blackwell Publishing Asia
Issue Date: 2010
ISSN: 1756-1841
1756-185X
Statement of
Responsibility: 
Sally Cox, Vidya Limaye, Catherine Hill, Peter Blumbergs and Peter Roberts-Thomson
Abstract: Idiopathic inflammatory myopathies (IIM) are a group of rare autoimmune disorders characterized by muscle inflammation and progressive weakness. The cause of IIM is unclear but it is believed that disease expression may be triggered by unknown factors in genetically predisposed individuals. Diagnosis is based on a combination of clinical, laboratory and electromyography findings. Muscle biopsy is the definitive diagnostic test. Research into IIM has been limited by the rarity of the disease, a somewhat insidious onset, difficulties with classification and diagnostic methods and heterogeneous study populations making cross-study evaluations difficult. This paper reviews the diagnostic and classification criteria of the IIM and examines epidemiological studies that have been performed, focusing on demographics.
Keywords: classification; diagnosis; epidemiology; idiopathic inflammatory myositis.
Rights: © 2010 Asia Pacific League of Associations for Rheumatology and Blackwell Publishing Asia Pty Ltd.
RMID: 0020097454
DOI: 10.1111/j.1756-185X.2010.01472.x
Appears in Collections:Pathology publications

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