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The Intractable Puzzle of Sporadic Creutzfeldt-Jakob Disease in Very Young People
Neurology ( IF 7.7 ) Pub Date : 2021-10-26 , DOI: 10.1212/wnl.0000000000012739
Simon Mead 1
Affiliation  

In the era of randomized controlled trials and multicenter observational studies, it is easy for academic neurology to overlook the compelling questions posed by individual patient cases. Sporadic Creutzfeldt-Jakob disease (sCJD) in a 21-year-old patient was the right diagnosis, but hardly a satisfactory explanation for either the doctor or patient and his family in the Clinical/Scientific Note by Appleby et al.1 in this week's issue of Neurology®. How can a typically late-onset disorder occur in someone so young?



中文翻译:

非常年轻的散发性克雅氏病的棘手难题

在随机对照试验和多中心观察研究的时代,学术神经学很容易忽视个别患者病例提出的令人信服的问题。一名 21 岁患者的散发性克雅氏病 (sCJD) 是正确的诊断,但在 Appleby 等人的《临床/科学说明》中,对于医生或患者及其家人来说,这很难令人满意的解释。1在本周一期的Neurology®中。这么年轻的人怎么会出现典型的迟发性疾病?

更新日期:2021-10-26
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