Systemic-onset juvenile idiopathic arthritis: the changing life of a rare disease.

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Version: author
Serval ID
serval:BIB_E8DDE80F9FF8
Type
Article: article from journal or magazin.
Publication sub-type
Review (review): journal as complete as possible of one specific subject, written based on exhaustive analyses from published work.
Collection
Publications
Institution
Title
Systemic-onset juvenile idiopathic arthritis: the changing life of a rare disease.
Journal
Swiss Medical Weekly
Author(s)
Cimaz R., Von Scheven A., Hofer M.
ISSN
1424-3997 (Electronic)
ISSN-L
0036-7672
Publication state
Published
Issued date
2012
Volume
142
Pages
w13582
Language
english
Notes
Publication types: Journal Article ; Review Publication Status: epublish
Abstract
Systemic-onset juvenile idiopathic arthritis (SoJIA), sometimes called Still's disease, is a systemic inflammatory disease classified within the spectrum of juvenile idiopathic arthritis (JIA). It is an orphan disease with often a chronic course and a major impact on the affected children and their families. This disorder is unique in terms of clinical manifestations, prognosis and response to conventional immunosuppressants. The objectives of this review are to describe SoJIA and emphasise the recent advances in the pathogenesis and treatment, which have transformed the care and the prognosis of this potentially life-threatening paediatric condition.
Pubmed
Web of science
Open Access
Yes
Create date
09/06/2012 19:04
Last modification date
20/08/2019 17:11
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