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Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as  SH2...
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Updated: Apr 17, 2026

Synovial Fluid Analysis to Identify Osteoarthritis
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[Psoriatic rheumatism].

M Magub, J Sany

    La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
    |January 26, 1984
    PubMed
    Summary
    This summary is machine-generated.

    Psoriatic rheumatism, a chronic inflammatory joint disease in psoriasis patients, differs from rheumatoid arthritis and resembles ankylosing spondylitis. Its genetic links and immune dysfunction suggest shared origins, but the reason for joint involvement remains unclear.

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    Author Spotlight: Self-Assessment Protocol for Predicting Psoriatic Arthritis in Psoriasis Patients
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    Area of Science:

    • Rheumatology
    • Immunology
    • Genetics

    Context:

    • Psoriasis affects approximately 5% of patients with chronic inflammatory joint disease.
    • Psoriatic rheumatism is distinct from rheumatoid arthritis and shares features with ankylosing spondylitis.
    • It is classified within the seronegative spondylarthropathies group.

    Purpose:

    • To differentiate psoriatic rheumatism from rheumatoid arthritis.
    • To explore the genetic and immunologic factors contributing to psoriatic rheumatism.
    • To understand the pathogenesis of joint disease in psoriasis patients.

    Summary:

    • Psoriatic rheumatism is characterized by specific joint involvement patterns, negative serologic tests, and a generally less severe outcome compared to rheumatoid arthritis.
    • Axial involvement, including sacroiliitis and vertebral disease, is common, linking it to ankylosing spondylitis.
    • Genetic associations include HLA B27 for axial forms and HLA B17, B13, and B38 for other forms, similar to psoriasis genetics.

    Impact:

    • Highlights the distinct nature of psoriatic rheumatism within rheumatologic conditions.
    • Suggests a significant role for immunologic dysfunction in the development of both psoriasis and psoriatic rheumatism.
    • Identifies the need for further research into the etiological factors driving joint disease development in a subset of psoriasis patients.