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Capturing the Range of Disease Involvement in Localized Scleroderma: The Localized Scleroderma Total Severity Scale
Arthritis Care & Research ( IF 3.7 ) Pub Date : 2023-12-26 , DOI: 10.1002/acr.25281 Suzanne C Li 1 , C Egla Rabinovich 2 , Mara L Becker 2 , Kathryn S Torok 3 , Polly J Ferguson 4 , Fatma Dedeoglu 5 , Sandy Hong 6 , Vidya Sivaraman 7 , Ronald M Laxer 8 , Katie Stewart 9 , Maria F Ibarra 10 , Thomas Mason 11 , Gloria Higgins 7 , Elena Pope 8 , Xiaohu Li 12 , Tara Lozy 13 , Robert C Fuhlbrigge 14 ,
Arthritis Care & Research ( IF 3.7 ) Pub Date : 2023-12-26 , DOI: 10.1002/acr.25281 Suzanne C Li 1 , C Egla Rabinovich 2 , Mara L Becker 2 , Kathryn S Torok 3 , Polly J Ferguson 4 , Fatma Dedeoglu 5 , Sandy Hong 6 , Vidya Sivaraman 7 , Ronald M Laxer 8 , Katie Stewart 9 , Maria F Ibarra 10 , Thomas Mason 11 , Gloria Higgins 7 , Elena Pope 8 , Xiaohu Li 12 , Tara Lozy 13 , Robert C Fuhlbrigge 14 ,
Affiliation
Juvenile localized scleroderma (jLS) is a chronic autoimmune disease commonly associated with poor outcomes, including contractures, hemiatrophy, uveitis, and seizures. Despite improvements in treatment, >25% of patients with jLS have functional impairment. To improve patient evaluation, our workgroup developed the Localized scleroderma Total Severity Scale (LoTSS), an overall disease severity measure.
中文翻译:
捕捉局限性硬皮病的疾病受累范围:局部硬皮病总严重程度量表
幼年局限性硬皮病 (jLS) 是一种慢性自身免疫性疾病,通常与不良结局相关,包括挛缩、偏血、葡萄膜炎和癫痫发作。尽管治疗有所改善,但 >25% 的 jLS 患者存在功能障碍。为了改善患者评估,我们的工作组开发了局部硬皮病总严重程度量表 (LoTSS),这是一种整体疾病严重程度测量方法。
更新日期:2023-12-26
中文翻译:
捕捉局限性硬皮病的疾病受累范围:局部硬皮病总严重程度量表
幼年局限性硬皮病 (jLS) 是一种慢性自身免疫性疾病,通常与不良结局相关,包括挛缩、偏血、葡萄膜炎和癫痫发作。尽管治疗有所改善,但 >25% 的 jLS 患者存在功能障碍。为了改善患者评估,我们的工作组开发了局部硬皮病总严重程度量表 (LoTSS),这是一种整体疾病严重程度测量方法。