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[先天性代谢缺陷并非毫无希望;早期识别智力残疾儿童中可治疗的病症]

[Inborn errors of metabolism are not hopeless; early identification of treatable conditions in children with intellectual disability].

作者信息

van Karnebeek Clara D M

机构信息

Universiteit van British Columbia, afd. Kindergeneeskunde, Vancouver, Canada.

出版信息

Ned Tijdschr Geneeskd. 2014;158:A8042.

Abstract

Intellectual disability is a devastating condition affecting 2-3% of the global population; comorbidity is common. In addition to its lifelong impact on affected individuals, families and society as a whole, intellectual disability is associated with the highest healthcare costs of any disease. Inborn errors of metabolism constitute a group of rare genetic disorders that commonly manifest as an intellectual disability. For patients with these disorders, an increasing number of treatments are becoming available aimed at the pathophysiological mechanisms. A review of the literature identified 91 treatable inherited metabolic disorders; this was the basis for the development of a step-by-step diagnostic protocol and an app, Treatable-ID. A 2.5-year study in a tertiary setting treatable inborn errors of metabolism were identified as cause of intellectual disability in more than 5% of the children studied. It also showed that implementation of the diagnostic protocol reduced unnecessary costs and diagnostic delay. These results should motivate clinicians to aim diagnostic assessment of an individual with intellectual disability at treatable inborn errors of metabolism. Such an approach prevents brain damage, improves development and health and gives patients hope.

摘要

智力残疾是一种影响全球2%至3%人口的严重疾病;合并症很常见。除了对受影响的个体、家庭和整个社会产生终身影响外,智力残疾在所有疾病中医疗成本最高。先天性代谢缺陷是一组罕见的遗传疾病,通常表现为智力残疾。对于患有这些疾病的患者,越来越多针对病理生理机制的治疗方法可供使用。一项文献综述确定了91种可治疗的遗传性代谢疾病;这是逐步诊断方案和一款名为Treatable-ID的应用程序得以开发的基础。在一家三级医疗机构进行的为期2.5年的研究中,可治疗的先天性代谢缺陷被确定为超过5%的研究儿童智力残疾的原因。研究还表明,实施诊断方案可降低不必要的成本并减少诊断延迟。这些结果应促使临床医生将对智力残疾个体的诊断评估目标设定为可治疗的先天性代谢缺陷。这种方法可预防脑损伤、改善发育和健康状况,并给患者带来希望。

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