Gerstmann-Straussler-Scheinker syndrome masquerading multiple sclerosis

被引:6
作者
Karmon, Yuval [1 ]
Kurzweil, Arielle [2 ]
Lindzen, Eric
Holmlund, Tomas [3 ]
Weinstock-Guttman, Bianca
机构
[1] SUNY Buffalo, Jacobs Neurol Inst, Sch Med & Biomed Sci, Baird MS Ctr, Buffalo, NY 14260 USA
[2] NYU, Sch Med, New York, NY 10003 USA
[3] SUNY Buffalo, Dent Neurol Inst, Sch Med & Biomed Sci, Buffalo, NY 14260 USA
关键词
Gerstmann-Straussler-Scheinker syndrome; Multiple sclerosis; MRI; Prion; CSF oligoclonal bands; CODON; 129; DISEASE; HETEROGENEITY; MUTATION; PRNP;
D O I
10.1016/j.jns.2011.07.028
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Gerstmann-Straussler-Scheinker syndrome (GSS) is a rare degenerative disorder of the central nervous system that belongs to the family of human spongiform encephalopathies, or prion diseases. GSS is almost always inherited and mostly carried in an autosomal dominant pattern. Nevertheless. GSS is genetically and phenotypically heterogeneous; among the different prion diseases GSS has the longest clinical course thereby has the potential to mimic the clinical course of different neurological disorders. Here, we report of a patient with a progressive ataxic syndrome, with MRI and CSF findings suggestive of a demyelinating-inflammatory process as multiple sclerosis and the cues that prompted to a final diagnosis of GSS. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:55 / 57
页数:3
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