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携带V180I突变的克雅氏病的临床特征。

Clinical features of Creutzfeldt-Jakob disease with V180I mutation.

作者信息

Jin K, Shiga Y, Shibuya S, Chida K, Sato Y, Konno H, Doh-ura K, Kitamoto T, Itoyama Y

机构信息

Department of Neurology, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Neurology. 2004 Feb 10;62(3):502-5. doi: 10.1212/01.wnl.0000106954.54011.80.

Abstract

The authors describe the clinical features of Creutzfeldt-Jakob disease (CJD) with the causative point mutation at codon 180. The symptoms never started with visual or cerebellar involvement. The patients showed slower progression of the disease compared with sporadic CJD. They never showed periodic sharp and wave complexes in EEG. MRI demonstrated remarkable high-intensity areas with swelling in the cerebral cortex except for the medial occipital and cerebellar cortices. These characteristic MRI findings are an important clue for an accurate premortem diagnosis.

摘要

作者描述了第180密码子存在致病性点突变的克雅氏病(CJD)的临床特征。症状从未以视觉或小脑受累开始。与散发性CJD相比,这些患者的疾病进展较慢。他们的脑电图从未出现周期性锐波复合波。磁共振成像(MRI)显示,除枕叶内侧和小脑皮质外,大脑皮质有明显的高强度肿胀区域。这些特征性的MRI表现是准确进行生前诊断的重要线索。

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