| Literature DB >> 28131204 |
Atsuhiko Sugiyama1, Noriko Sato2, Yukio Kimura1, Tomoko Maekawa1, Noritaka Wakasugi3, Daichi Sone1, Mikako Enokizono1, Yuji Takahashi3, Miho Murata3, Hidehiro Mizusawa3, Hiroshi Matsuda4.
Abstract
Gerstmann-Sträussler-Scheinker syndrome caused by the P102L mutation in the prion protein gene (GSS102) is usually characterized by the onset of slowly progressive cerebellar ataxia, with dementia occurring much later. Because of the relatively long disease course and the prominence of progressive cerebellar ataxia in the early stage, GSS102 is often misdiagnosed as other neurodegenerative disorders. We present two cases of genetically proven GSS102L, both of which present with atrophy and decreased blood flow of the thalamus as determined by voxel-based specific regional analysis system for Alzheimer's disease (VSRAD) advance software and easy Z-score analysis for 99mTc-ethyl cysteinate dimer-SPECT, respectively. These thalamic abnormalities have not been fully evaluated to date, and detecting them might be useful for differentiating GSS102 from other neurodegenerative disorders.Entities:
Keywords: Easy Z-score analysis; MRI; P102L; SEPCT; VSRAD
Mesh:
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Year: 2016 PMID: 28131204 DOI: 10.1016/j.jns.2016.12.021
Source DB: PubMed Journal: J Neurol Sci ISSN: 0022-510X Impact factor: 3.181