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Juvenile Idiopathic Arthritis: Etiopathogenesis, Therapy And Outcomes

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dc.contributor.author Karimdzhanov, I.A.
dc.contributor.author Iskanova, G. KH.
dc.contributor.author Israilova, N.A.
dc.date.accessioned 2023-10-12T06:51:06Z
dc.date.available 2023-10-12T06:51:06Z
dc.date.issued 2023
dc.identifier.uri http://repository.tma.uz/xmlui/handle/1/9173
dc.description.abstract Juvenile idiopathic arthritis (JIA) is the most common rheumatological disease in children and is classified according to the criteria of the International League of Rheumatological Associations. JIA is divided into oligoarticular, polyarticular, systemic, psoriatic, enthesitis-like, and undifferentiated arthritis, depending on the number of affected joints, the presence of extra-articular manifestations, systemic symptoms, serological changes, and genetic factors. This article provides an overview of advances in understanding JIA pathogenesis, etiology, histopathology, immunological changes consistent with disease activity, and treatment options. JIA is discussed in the context of treatment, including traditional non-biological and modern biologic antirheumatic drugs. However, a significant number of patients remain refractory to treatment, although the advent of advanced therapeutic methods has improved clinical outcomes, which necessitates further understanding of the progression and remission of the disease in order to select adequate therapy en_US
dc.language.iso en en_US
dc.subject juvenile idiopathic arthritis, pathogenesis of juvenile idiopathic arthritis, etiology of juvenile idiopathic arthritis, antirheumatic drug therapy en_US
dc.title Juvenile Idiopathic Arthritis: Etiopathogenesis, Therapy And Outcomes en_US
dc.type Thesis en_US


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