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首页> 外文会议>Mediterranean Conference on Medical and Biological Engineering and Computing >Methods for Personalized Diagnostics
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Methods for Personalized Diagnostics

机译：个性化诊断方法

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摘要

Historically medical diagnosis has relied on observation of signs and symptom followed by comparison of these signs and symptoms to profiles of known instances of the disease. While this approach works well in straight-forward diagnosis in commonly found diseases it may not work well for rare diseases or for a common disease that does not present with the normal symptom pattern or when symptoms are the result of the presence of more than one disease. New technologies can assist in the diagnostic process through a number of paradigms, including examination of the life-long patient history, analysis of genetics components, and the inclusion of multidimensional medical decision making that makes full use of automated scanning and analysis. In this article specific approaches that can contribute to personal diagnosis are coupled with a structure for maintaining life-long patient and family history data.
机译：历史上医学诊断依赖于观察症状和症状，然后将这些迹象和症状与已知病例的概况进行比较。虽然这种方法在常见的疾病中，在公然发现的疾病中良好良好，但对于罕见疾病或常规症状模式不存在的常见疾病或症状是存在多种疾病的结果时，它可能无法正常工作。新技术可以通过许多范式协助诊断过程，包括检查终身患者历史，遗传分析分析，并包含多维医学决策，充分利用自动扫描和分析。在本文中，可以促进个人诊断的具体方法与维护终身患者和家族历史数据的结构相结合。

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