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

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Date

2012

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Serveur académique Lausannois

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Ce document est lié à :
info:eu-repo/semantics/altIdentifier/doi/10.4414/smw.2012.13582

Ce document est lié à :
info:eu-repo/semantics/altIdentifier/pmid/22573189

Ce document est lié à :
info:eu-repo/semantics/altIdentifier/eissn/1424-3997

Ce document est lié à :
info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_E8DDE80F9FF88

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Serveur Académique Lausannois

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Université de Lausanne et CHUV

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info:eu-repo/semantics/openAccess , Copying allowed only for non-profit organizations , https://serval.unil.ch/disclaimer

Sujets proches En

Joints--Inflammation Arthritides illness

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R. Cimaz et al., « Systemic-onset juvenile idiopathic arthritis: the changing life of a rare disease. », Serveur académique Lausannois, ID : 10.4414/smw.2012.13582

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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.

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