Deafness: an unusual onset of genetic Crewtzfeldt-Jakob disease

被引：15

作者：

Cataldi, ML ^{[1
]}

Restivo, O ^{[1
]}

Reggio, E ^{[1
]}

Restivo, DA ^{[1
]}

Reggio, A ^{[1
]}

机构：

[1] Univ Catania, Dept Neurol Sci, I-95125 Catania, Italy

来源：

NEUROLOGICAL SCIENCES | 2000年 / 21卷 / 01期

关键词：

genetic Creutzfeldt-Jakob disease; deafness; MRI; 14-3-3; protein;

D O I：

10.1007/s100720070119

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

We describe a case of genetic Creutzfeldt-Jakob disease (CJD) with deafness at the onset. We report clinical features, 14-3-3 protein positivity, electroencephalography and brain stem auditory evoked potential abnormalities, and high signal on magnetic resonance imaging in basal ganglia and temporal cortex. Similarities with CJD Heidenhain variant are discussed.

引用

页码：53 / 55

页数：3

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