面向初级保健医生的艾勒斯-丹洛斯多动症。

Missouri medicine Pub Date : 2024-07-01
Laura White, Sara S Procknow
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引用次数: 0

摘要

关节活动过度和关节痛在普通人群中非常常见。患者和医疗服务提供者对关节活动过度症和活动过度埃勒斯-丹洛斯综合症(hEDS)的认识不断提高,导致评估需求激增。许多活动过度症患者都符合活动过度谱系障碍(HSD)或活动过度丹洛斯综合征(hEDS)的临床诊断标准,但单基因结缔组织病(CTD)却很少见。除非怀疑存在其他潜在的 CTD,否则不建议对 HSD/hEDS 患者进行基因检测。鉴于 HSD/hEDS 在普通人群中的高发病率,初级保健提供者应熟悉 HSD/hEDS 的评估、管理和转诊至 CTD 专家的指征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hypermobile Ehlers Danlos for the Primary Care Provider.

Joint hypermobility is very common in the general population as is arthralgia. Increased awareness of hypermobility and hypermobile Ehlers Danlos Syndrome (hEDS) among patients and providers has led to a surge in demand for evaluation. Many patients with hypermobility meet clinical criteria for a diagnosis of hypermobile spectrum disorder (HSD) or hEDS, but monogenic connective tissue diseases (CTD) are rare. Genetic testing is not recommended for patients with HSD/hEDS unless another underlying CTD is suspected. Given the high prevalence of HSD/hEDS in the general population, primary care providers should be familiar with HSD/hEDS evaluation, management, and indication for referral to a CTD specialist.

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CiteScore
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