Juvenile dermatomyositis. Where are we now?

Juvenile onset idiopathic inflammatory myopathy (IIM) has many similarities and distinct differences from adult-onset disease. This review will focus on recent developments in understanding and treatment of juvenile dermatomyositis (JDM), the most common disease sub-type of IIM in childhood. JDM is...

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Veröffentlicht in:Clinical and Experimental Rheumatology 2022-02, Vol.40 (2), p.394-403
Hauptverfasser: McCann, Liza J, Livermore, Polly, Wilkinson, Meredyth G Ll, Wedderburn, Lucy R
Format: Artikel
Sprache:eng
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Zusammenfassung:Juvenile onset idiopathic inflammatory myopathy (IIM) has many similarities and distinct differences from adult-onset disease. This review will focus on recent developments in understanding and treatment of juvenile dermatomyositis (JDM), the most common disease sub-type of IIM in childhood. JDM is a systemic immune mediated vasculopathy, increasingly recognised as a group of distinct phenotypes with variable presentation and outlook. This overview will describe long-term outlook and disease course including health-related quality of life and emerging treatments.
ISSN:0392-856X
1593-098X
DOI:10.55563/clinexprheumatol/56ilob