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国际疑难病诊治网络:五年及以上!

The Undiagnosed Diseases Network International: Five years and more!

机构信息

National Centre for Rare Diseases, Undiagnosed Rare Diseases Interdepartmental Unit, Istituto Superiore di Sanità, Rome, Italy.

Western Australian Register of Developmental Anomalies and Genetic Services of WA, WA Health Department, Perth, Australia; Faculty of Health and Medical Sciences, Division of Paediatrics and Telethon Kids Institute, Perth, Australia.

出版信息

Mol Genet Metab. 2020 Apr;129(4):243-254. doi: 10.1016/j.ymgme.2020.01.004. Epub 2020 Jan 17.

Abstract

Undiagnosed rare diseases (URDs) account for a significant portion of the overall rare disease burden, depending upon the country. Hence, URDs represent an unmet medical need. A specific challenge posed by the ensemble of the URD patient cohort is the heterogeneity of its composition; the group, indeed, includes very rare, still unidentified conditions as well as clinical variants of recognized rare diseases. Exact disease recognition requires new approaches that cut across national and institutional boundaries, may need the implementation of methods new to diagnostics, and embrace clinical care and research. To address these issues, the Undiagnosed Diseases Network International (UDNI) was established in 2014, with the major aims of providing diagnoses to patients, implementing additional diagnostic tools, and fostering research on novel diseases, their mechanisms, and their pathways. The UDNI involves centres with internationally recognized expertise, and its scientific resources and know-how aim to fill the knowledge gaps that impede diagnosis, in particularly for ultra-rare diseases. Consequently, the UDNI fosters the translation of research into medical practice, aided by active patient involvement. The goals of the UDNI are to work collaboratively and at an international scale to: 1) provide diagnoses for individuals who have conditions that have eluded diagnosis by clinical experts; 2) gain insights into the etiology and pathogenesis of novel diseases; 3) contribute to standards of diagnosing unsolved patients; and 4) share the results of UDNI research in a timely manner and as broadly as possible.

摘要

未确诊的罕见病(URD)在整体罕见病负担中占很大比例,具体比例取决于国家。因此,URD 代表了未满足的医疗需求。URD 患者群体所面临的一个特殊挑战是其组成的异质性;该群体确实包括非常罕见、尚未确定的疾病以及已确认的罕见病的临床变异。准确识别疾病需要新的方法,这些方法需要跨越国家和机构的界限,可能需要实施新的诊断方法,并涵盖临床护理和研究。为了解决这些问题,未确诊疾病网络国际组织(UDNI)于 2014 年成立,其主要目标是为患者提供诊断,实施额外的诊断工具,并促进对新疾病及其机制和途径的研究。UDNI 涉及具有国际公认专业知识的中心,其科学资源和专业知识旨在填补阻碍诊断的知识空白,特别是针对超罕见疾病。因此,UDNI 通过积极的患者参与,促进了研究向医疗实践的转化。UDNI 的目标是在国际范围内合作:1)为那些被临床专家诊断为疑难杂症的患者提供诊断;2)深入了解新疾病的病因和发病机制;3)为未解决患者的诊断标准做出贡献;4)及时并尽可能广泛地分享 UDNI 研究成果。

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