InGene 2.0: a step towards the ICT-based diagnosis and monitoring of neuromuscular disorders

Francesco Sansone, A. Tonacci, G. Astrea, A. Rubegni, F. Santorelli, Raffaele Conte
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Abstract

In the universe of neuromuscular disorders (NMD), a peculiar feature is represented by the amount of rare NMDs, singularly accounting for a relatively scarce number of individuals, but representing huge records when taken together. The main clinical problem with rare NMDs deals with their correct diagnosis, which is difficult due to their similar phenotypes, and with the correct choice towards their treatment, which is key to successfully improve the patients’ health status. In this regard, it is essential to promote the collection of data in a structured, user-friendly manner for clinicians, at the same time keeping it usable for data scientists and researchers in the field. Information and Communication Technologies (ICT) are fundamental in this regard, making it possible to achieve this ambitious goal. The InGene 2.0 project is therefore aimed at setting up a safe, secure, GDPR-compliant, ICT-based software platform to collect multimodal, multiparametric data in this regard, entering the market of NMDs with useful tools for both the clinicians and data scientists.
InGene 2.0:迈向基于信息通信技术的神经肌肉疾病诊断和监测的一步
在神经肌肉疾病(NMD)的世界中,罕见NMD的数量代表了一个特殊的特征,奇怪的是,它们只占相对稀少的个体数量,但当它们加在一起时,却代表了巨大的记录。罕见nmd临床面临的主要问题是,由于其表型相似,难以正确诊断,正确选择治疗方法是成功改善患者健康状况的关键。在这方面,促进临床医生以结构化、用户友好的方式收集数据是至关重要的,同时保持数据科学家和该领域的研究人员可用。信息和通信技术(ICT)是这方面的基础,使实现这一宏伟目标成为可能。因此,InGene 2.0项目旨在建立一个安全、可靠、符合gdpr、基于ict的软件平台,以收集这方面的多模式、多参数数据,为临床医生和数据科学家提供有用的工具,进入nmd市场。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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