PDF(Pubmed)
Abstract：
Creutzfeldt-Jakob disease (CJD) is a very rare neurodegenerative disorder that usually presents as rapidly progressive dementia with an extremely poor prognosis. The diagnosis of CJD can be extremely challenging due to its rarity, manifestation with non-specific neurological symptoms, associated broad differentials, and a need for extensive workup. Awareness of disease-specific biomarkers, radiological signs, and diagnostic criteria are crucial for timely diagnosis. Here, we report a case of CJD, which presented as an atypical movement disorder that progressed to dementia and failure to thrive within a few weeks of presentation.
摘要：
克雅氏病（CJD）是一种非常罕见的神经退行性疾病，通常表现为快速进行性痴呆，预后极差。由于CJD的稀有性，CJD的诊断可能极具挑战性，表现为非特异性神经症状，相关的广泛差异，需要广泛的检查。对疾病特异性生物标志物的认识，放射征象,诊断标准对及时诊断至关重要。这里,我们报告了一例CJD,表现为一种非典型的运动障碍，在出现后的几周内进展为痴呆症，无法茁壮成长。
