Literature DB >> 11196366

The CINCA syndrome: a rare cause of chronic arthritis and multisystem inflammatory disorders.

H de Boeck1, T Scheerlinck, J Otten.   

Abstract

Chronic infantile neurological cutaneous articular (CINCA) syndrome is a rare disorder with neonatal onset characterised by a chronic progressive inflammatory process with skin rash, articular and central nervous system involvement. This primary systemic inflammatory disorder should be distinguished from juvenile rheumatoid arthritis (JRA). Although the articular findings are characteristic features of CINCA syndrome, there is a certain degree of variability in the articular involvements which are not always symmetrical nor is the degree of severity uniform. The etiology of CINCA syndrome remains unknown. No single treatment has been found to be effective. This syndrome is known in the American medical literature as infantile onset multisystem inflammatory disease (IOMID).

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Year:  2000        PMID: 11196366

Source DB:  PubMed          Journal:  Acta Orthop Belg        ISSN: 0001-6462            Impact factor:   0.500


  2 in total

1.  Anakinra in mutation-negative CINCA syndrome.

Authors:  José Luis Callejas; Javier Oliver; Javier Martín; Norberto Ortego
Journal:  Clin Rheumatol       Date:  2006-01-27       Impact factor: 2.980

2.  Long-term response after 6-year treatment with anakinra and onset of focal bone erosion in neonatal-onset multisystem inflammatory disease (NOMID/CINCA).

Authors:  Donato Rigante; Antonio Leone; Raffaella Marrocco; Maria Elena Laino; Achille Stabile
Journal:  Rheumatol Int       Date:  2011-01-15       Impact factor: 2.631

  2 in total

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