Institute of Neurology, Catholic University of Sacred Heart, Rome, Italy.
Neurol Sci. 2010 Dec;31(6):837-9. doi: 10.1007/s10072-010-0388-0. Epub 2010 Aug 21.
E200K mutation of the prion protein gene (PRNP) presented with a variety of phenotypes. A 55-year-old woman complaining of slowly progressive walking difficulties came to our observation. She showed a severe progressive ataxo-spastic syndrome but a mild cognitive impairment only. Repeated EEGs showed a diffuse slowing of the rhythm without specificity. Brain MRI revealed by FLAIR showed widespread multiple hyperintensities in the whole cerebral cortex, caudate and putamen nuclei, and in the pulvinar and medial thalamus bilaterally. These signal abnormalities were best detected by DWI with restricted diffusion on ADC map. The clinical diagnosis of possible genetic Creutzfeldt-Jakob disease (CJD) has been confirmed by PRNP gene analysis which revealed the presence of a E200K mutation. This report confirms the heterogeneity of phenotypes in E200K mutated familial CJD with the occurrence of a new phenotype not previously described.
朊蛋白基因(PRNP)E200K 突变呈现出多种表型。一位 55 岁的女性因进行性行走困难前来就诊。她表现出严重的进行性共济失调痉挛综合征,但仅有轻度认知障碍。重复脑电图显示节律弥漫性减慢,无特异性。FLAIR 脑 MRI 显示整个大脑皮层、尾状核和壳核以及双侧丘脑枕和内侧丘脑广泛多发高信号。这些信号异常在 DWI 上显示受限扩散的 ADC 图上最佳。PRNP 基因分析证实可能的遗传性克雅氏病(CJD)的临床诊断,该分析显示存在 E200K 突变。本报告证实了 E200K 突变家族性 CJD 表型的异质性,出现了以前未描述的新表型。