Equity in action: The Diagnostic Working Group of The Undiagnosed Diseases Network International.

IF 4.7 2区 医学 Q1 GENETICS & HEREDITY NPJ Genomic Medicine Pub Date : 2024-07-05 DOI:10.1038/s41525-024-00422-y
Elizabeth Emma Palmer, Helene Cederroth, Mikk Cederroth, Angelica Maria Delgado-Vega, Natalie Roberts, Fulya Taylan, Ann Nordgren, Lorenzo D Botto
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Abstract

Rare diseases are recognized as a global public health priority. A timely and accurate diagnosis is a critical enabler for precise and personalized health care. However, barriers to rare disease diagnoses are especially steep for those from historically underserved communities, including low- and middle-income countries. The Undiagnosed Diseases Network International (UDNI) was launched in 2015 to help fill the knowledge gaps that impede diagnosis for rare diseases, and to foster the translation of research into medical practice, aided by active patient involvement. To better pursue these goals, in 2021 the UDNI established the Diagnostic Working Group of the UDNI (UDNI DWG) as a community of practice that would (a) accelerate diagnoses for more families; (b) support and share knowledge and skills by developing Undiagnosed Diseases Programs, particularly those in lower resource areas; and (c) promote discovery and expand global medical knowledge. This Perspectives article documents the initial establishment and iterative co-design of the UDNI DWG.

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公平在行动:国际未诊断疾病网络诊断工作组。
罕见病是公认的全球公共卫生优先事项。及时准确的诊断是实现精确和个性化医疗保健的关键因素。然而,对于那些来自历来得不到充分服务的社区(包括低收入和中等收入国家)的人来说,罕见病诊断的障碍尤其严重。国际未确诊疾病网络(UDNI)于 2015 年启动,旨在帮助填补阻碍罕见病诊断的知识空白,并在患者积极参与的帮助下,促进将研究成果转化为医疗实践。为了更好地实现这些目标,UDNI 于 2021 年成立了 UDNI 诊断工作组(UDNI DWG),作为一个实践社区,该工作组将:(a) 加快对更多家庭的诊断;(b) 通过制定未确诊疾病计划,尤其是资源较少地区的未确诊疾病计划,支持并分享知识和技能;(c) 促进发现并扩展全球医学知识。这篇《视角》文章记录了 UDNI DWG 的初步建立和反复共同设计。
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来源期刊
NPJ Genomic Medicine
NPJ Genomic Medicine Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
9.40
自引率
1.90%
发文量
67
审稿时长
17 weeks
期刊介绍: npj Genomic Medicine is an international, peer-reviewed journal dedicated to publishing the most important scientific advances in all aspects of genomics and its application in the practice of medicine. The journal defines genomic medicine as "diagnosis, prognosis, prevention and/or treatment of disease and disorders of the mind and body, using approaches informed or enabled by knowledge of the genome and the molecules it encodes." Relevant and high-impact papers that encompass studies of individuals, families, or populations are considered for publication. An emphasis will include coupling detailed phenotype and genome sequencing information, both enabled by new technologies and informatics, to delineate the underlying aetiology of disease. Clinical recommendations and/or guidelines of how that data should be used in the clinical management of those patients in the study, and others, are also encouraged.
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