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  2. Volume 9, Issue 7
  3. Author

Online ISSN: 2515-8260

Volume9, Issue7

A Case of Idiopathic Inflammatory Polymyositis – a rare phenomenon

    Dr G S Sanjay Surya Dr Priya Venugopalan Dr Gowtham Hanumanram Dr Kannan Rajendran Dr Gowrishankar A

European Journal of Molecular & Clinical Medicine, 2022, Volume 9, Issue 7, Pages 2412-2415

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Abstract

Idiopathic inflammatory polymyositis is a disorder characterised by progressive muscle weakness, extra muscular manifestations , elevated serum levels of muscle enzymes , Electromyographic (EMG) abnormalities, inflammatory infiltrates in muscle biopsy . Extra muscular involvement such as pulmonary , cardiac and gastrointestinal involvement is correlated with increased mortality and morbidity in patients. Here we report a case of idiopathic inflammatory polymyositis.
Keywords:
    Polymyositis Anti JO-1 antibodies idiopathic inflammatory polymyositis IIM
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(2022). A Case of Idiopathic Inflammatory Polymyositis – a rare phenomenon. European Journal of Molecular & Clinical Medicine, 9(7), 2412-2415.
Dr G S Sanjay Surya Dr Priya Venugopalan Dr Gowtham Hanumanram Dr Kannan Rajendran Dr Gowrishankar A. "A Case of Idiopathic Inflammatory Polymyositis – a rare phenomenon". European Journal of Molecular & Clinical Medicine, 9, 7, 2022, 2412-2415.
(2022). 'A Case of Idiopathic Inflammatory Polymyositis – a rare phenomenon', European Journal of Molecular & Clinical Medicine, 9(7), pp. 2412-2415.
A Case of Idiopathic Inflammatory Polymyositis – a rare phenomenon. European Journal of Molecular & Clinical Medicine, 2022; 9(7): 2412-2415.
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