Inflammatory spondyloarthritis (Q44409): Difference between revisions

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Espondiloartrites inflamatórias são um grupo de doenças reumáticas inflamatórias, caracterizadas pela presença de comprometimento articular inflamatório axial e periférico (preferencialmente de membros inferiores), entesite, dactilite e uveíte. As manifestações clínicas são a ocorrência de comprometimento axial sob a forma de espondilite ou sacroiliíte, associada ou não à artrite periférica assimétrica predominante em membros inferiores, dactilites, entesites ou uveíte anterior aguda. Há uma marcante agregação familiar e a associação com o HLA-B27 e ausência do fator reumatoide, de nódulos subcutâneos ou de outras manifestações extra-articulares da artrite reumatoide.
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Inflammatory spondyloarthritis is a rheumatic disease referring to the group of inflammatory disorders affecting the lower limb, enthesitis, dactylitis, and uveitis. Clinical characteristics include typical patterns of peripheral arthritis (i.e., predominantly of the lower limb and asymmetric), absence of rheumatoid factor, absence of subcutaneous nodules and other extra-articular features of rheumatoid arthritis, overlapping extra-articular features of the group (e.g., anterior uveitis), and significant familial aggregation and association with HLA-B27.

Revision as of 11:51, 13 August 2026

Inflammatory spondyloarthritis is a rheumatic disease referring to the group of inflammatory disorders affecting the lower limb, enthesitis, dactylitis, and uveitis. Clinical characteristics include typical patterns of peripheral arthritis (i.e., predominantly of the lower limb and asymmetric), absence of rheumatoid factor, absence of subcutaneous nodules and other extra-articular features of rheumatoid arthritis, overlapping extra-articular features of the group (e.g., anterior uveitis), and significant familial aggregation and association with HLA-B27.
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    English
    Inflammatory spondyloarthritis
    Inflammatory spondyloarthritis is a rheumatic disease referring to the group of inflammatory disorders affecting the lower limb, enthesitis, dactylitis, and uveitis. Clinical characteristics include typical patterns of peripheral arthritis (i.e., predominantly of the lower limb and asymmetric), absence of rheumatoid factor, absence of subcutaneous nodules and other extra-articular features of rheumatoid arthritis, overlapping extra-articular features of the group (e.g., anterior uveitis), and significant familial aggregation and association with HLA-B27.

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