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166 Possible Causes for Secondary Amyloidosis, Systemic Juvenile Idiopathic Arthritis

  • Cryopyrin-Associated Periodic Syndrome

    In May 2013, it was also approved for the treatment of active Systemic Juvenile Idiopathic Arthritis (SJIA) in patients aged 2 through 16 years.[rarediseases.info.nih.gov] Response (Luis Bolaños): AA amyloid material is the precursor protein to secondary or reactive amyloidosis.[revistanefrologia.com] Also approved for the treatment of active Systemic Juvenile Idiopathic Arthritis (SJIA) in patients aged 2 through 16 years.[checkorphan.org]

  • Juvenile Seronegative Polyarthritis

    juvenile idiopathic arthritis.[ped-rheum.biomedcentral.com] Of the secondary amyloidosis patients, 29 out of 51 carried HLA B27.[link.springer.com] Secondary amyloidosis. Joint destruction - over 50% of children with chronic systemic JIA require joint surgery. Osteoporosis.[patient.info]

  • Adult-Onset Still Disease

    The characteristic rash of systemic juvenile idiopathic arthritis is a transient erythematous eruption associated with a quotidian spiking fever.[ncbi.nlm.nih.gov] Some patients may develop secondary amyloidosis due to the chronic inflammatory state.[clinicaladvisor.com] ISSN 1546-0096 Abstract Background: Adult-onset Still’s disease (AOSD), a rare autoinflammatory disorder, resembles systemic juvenile idiopathic arthritis (SJIA).[ub.uni-heidelberg.de]

  • Muckle-Wells Syndrome

    juvenile idiopathic arthritis.[guidetopharmacology.org] Response (Luis Bolaños): AA amyloid material is the precursor protein to secondary or reactive amyloidosis.[revistanefrologia.com] juvenile idiopathic arthritis (SJIA).[drugbank.ca]

  • CINCA Syndrome

    juvenile idiopathic arthritis (SJIA) are rare systemic disorders of auto-inflammatory nature.[sobi.com] Secondary amyloidosis can appear. Etiology Mutations in the CIAS1 gene have been identified in 60% of patients with either the sporadic or familial forms.[orpha.net] […] onset juvenile idiopathic arthritis which shares many aspects with CINCA but it is rare in the first 6 months of life.[medcraveonline.com]

  • Inflammatory Bowel Disease

    juvenile idiopathic arthritis (JIA); Crohn's disease; and ulcerative colitis.[ncbi.nlm.nih.gov] The reported cases of secondary amyloidosis in children with IBD are much fewer than those reported in adults.[ncbi.nlm.nih.gov] Inflammatory bowel disease can develop in the context of some rheumatic diseases in childhood, including juvenile idiopathic arthritis (JIA).[ncbi.nlm.nih.gov]

  • Juvenile Rheumatoid Arthritis

    S: Systemic Whole body is affected J: Juvenile Begins in childhood I: Idiopathic Cause is unknown A: Arthritis Joint inflammation SJIA (systemic juvenile idiopathic arthritis[periodicfevers.com] Secondary amyloidosis. Joint destruction - over 50% of children with chronic systemic JIA require joint surgery. Osteoporosis.[patient.info] Some patients may develop secondary amyloidosis due to the chronic inflammatory state.[clinicaladvisor.com]

  • Renal Amyloidosis

    Abstract A 9-year-old girl presented with systemic-onset juvenile idiopathic arthritis, diagnosed at 3.5 of age and which was difficult to control despite several therapeutic[ncbi.nlm.nih.gov] Long standing RHD can lead to secondary AA amyloidosis.[ncbi.nlm.nih.gov] Inflammatory Arthritides Rheumatoid Arthritis Ankylosing Spondylitis Adult Still’s Disease Juvenile Idiopathic Arthritis Psoriatic Arthritis Gout Inflammatory Bowel Diseases[amyloidosis.org]

  • Rheumatoid Arthritis

    JIA 2016 EULAR/ACR/PRINTO Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis Complete Article Myositis Classification[rheumatology.org] Fernandez-Nebro A, Tomero E, Ortiz-Santamaria V et al. (2005) Treatment of rheumatic inflammatory disease in 25 patients with secondary amyloidosis using tumor necrosis factor[doi.org] De Benedetti F et al (2001) Effect of IL-6 on IGF binding protein-3: a study in IL-6 transgenic mice and in patients with systemic juvenile idiopathic arthritis.[dx.doi.org]

  • Tumor Necrosis Factor Receptor 1-associated Periodic Syndrome

    Juvenile Idiopathic Arthritis Autoinflammatory syndromes: diagnosis and management – a good synopsis of FMF, HIDS, TRAPS, CAPS, Blau Syndrome, PAPA Syndrome, PFAPA, and Majeed[saidsupport.org] Secondary amyloidosis complicates the course of the disease. The documents contained in this web site are presented for information purposes only.[orpha.net] Tumor necrosis factor receptor-associated periodic syndrome mimicking systemic juvenile idiopathic arthritis. Allergol Int 2006;55:337-41.[archivesofrheumatology.org]

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