首页> 外文期刊>American journal of medical genetics, Part A >Progressive polyepiphyseal dysplasia with arthropathy: A distinct disorder from idiopathic juvenile arthritis and pseudorheumatoid dysplasia?
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Progressive polyepiphyseal dysplasia with arthropathy: A distinct disorder from idiopathic juvenile arthritis and pseudorheumatoid dysplasia?

机译:患有关节炎的进行性多发性骨pi发育异常:与特发性青少年关节炎和假性类风湿性发育不良有明显区别吗?

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摘要

Juvenile idiopathic arthritis is an inflammatory disease with various onset-forms which can sometimes be difficult to distinguish from genetic inflammatory/rheumatoid-like osteoarthropathies. In this report, we describe two boys with severe chronic arthralgia, stiffness and swelling of joints, motor weakness and joints contractures evolving despite immunosuppressive treatments and for whom all biological and molecular exams failed to identify a prompt diagnosis. Some findings also overlap with pseudorheumatoid dysplasia but WISP3 gene molecular analysis failed to identify any mutation for both patients. Therefore, we propose that these boys show a clinical entity distinct from the actually known genetic inflammatory/rheumatoid-like osteoarthropathies.
机译:幼年特发性关节炎是一种具有多种发作形式的炎性疾病,有时可能难以与遗传性炎性/类风湿性关节炎类似的骨关节炎区分开。在本报告中,我们描述了两个患有严重慢性关节痛,关节僵硬和肿胀,运动无力和关节挛缩的男孩,尽管他们进行了免疫抑制治疗,但所有这些生物学和分子检查均未能明确诊断。一些发现也与假性类风湿性异常增生重叠,但是WISP3基因分子分析未能确定两名患者的任何突变。因此,我们建议这些男孩表现出不同于实际已知的遗传性炎症/类风湿性骨关节炎的临床表现。

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