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Prion Volume 12, 2018 - Issue 2
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Case Report

Wernicke-Korsakoff syndrome as a rare phenotype of sporadic Creutzfeldt-Jakob disease

Joanna BielewiczDepartment of Neurology, Medical University of Lublin, Lublin, PolandCorrespondence[email protected]
, MD, PhD,
Anna Szczepańska-SzerejDepartment of Neurology, Medical University of Lublin, Lublin, Poland
, MD, PhD,
Magdalena OgórekDepartment of Neurology, Medical University of Lublin, Lublin, Poland
, MD,
Piotr DropkoDepartment of Neurology, Medical University of Lublin, Lublin, Poland
, PhD,
Katarzyna WojtalDepartment of Interventional Radiology and Neuroradiology, Medical University of Lublin, Lublin, Poland
, MD, PhD &
Konrad RejdakDepartment of Neurology, Medical University of Lublin, Lublin, Poland
, MD, PhD
Pages 143-146 | Received 09 Oct 2017, Accepted 19 Jan 2018, Published online: 09 Feb 2018

References

  • Kovacs KG, Budka H. Prion diseases: from protein to cell pathology. Am J Pathol. 2008;172(3):555-565. doi:10.2353/ajpath.2008.070442. PMID:18245809.
  • World Health Organization. http://www.who.int/en/.
  • The National CJD Research and Surveillance Unit.http://www.cjd.ed.ac.uk/surveillance.
  • Snowden JS, Mann DM, Neary D. Distinct neuropsychological characteristics in Creutzfeld-Jakob disease. J Neurol Neurosurg Psychiatry. 2002;73(6):686-94. doi:10.1136/jnnp.73.6.686. PMID:12438471.
  • Gonzalez DA, Soble JR. Corticobasal syndrome due to sporadic Creutzfeldt-Jakob disease: a review and neuropsychological case report. Clin Neuropsychol. 2017;31(3): 676-689. doi:10.1080/13854046.2016.1259434. PMID:27871202.
  • Jcghin A, Devamecourt V, Bakchire S, et al. Unusual features of Creutzfeld-Jakob disease followed-up in a memory clinic. J Neurol. 2014;261(4):696-701. doi:10.1007/s00415-014-7246-6. PMID:24477491.
  • Baiardi S, Magherini A, Cappellari S, et al. Towards an early clinical diagnosis of sporadic CJDVV2. J Neurol Neurosurg Psychiatry. 2017;88(9):764-772. doi:10.1136/jnnp-2017-315942. PMID:28668775.
  • Al Balushi A, Meeks MW, Hayat G, et al. Creutzfeldt-Jakob Disease: Analysis of four cases. Front Neurol. 2016;29(7):138.
  • Choi YJ, Kang KW, Lee SY, et al. Creutzfeldt-Jakob disease presenting with and gaze-evoked nystagmus: a case report. Medicine (Baltimore). 2016;95(7):e2766. doi:10.1097/MD.0000000000002766. PMID:26886621.
  • Scalzo SJ, Bowden SC, Amrose ML, et al. Wernicke-Korsakoff syndrome not related to alcohol use: a systematic review. J Neurol Neurosurg Psychiatry. 2015;86(12):1362-8. PMID:25589780.
  • Chitronas N, Yung RS, Kofiskey DM, et al. Treatable neurological disorders misdiagnosed as Creutzfeldt-Jakob disease. Ann Neurol. 2011;70(3):437-44. doi:10.1002/ana.22454. PMID:21674591.
  • Lough ME. Wernicke's encephalopathy: expanding the diagnostic toolbox. Neuropsychol Rev. 2012;22(2): 181-94. doi:10.1007/s11065-012-9200-7. PMID:22577001.
  • Forner SA, Takada LT, Bettcher BM, et al. Comparing CSF biomarkersbrain MRI in the diagnosis of sporadic Creutzfeldt-Jakob disease. Neurol Clin Pract. 2015;5(2):116-125. doi:10.1212/CPJ.0000000000000111. PMID:26137420.
  • Liberski PP. Choroba Creutzfeldta i inne choroby wywołane przez priony – pasażowalne encefalopatie gąbczaste człowieka. Lublin: Wydawnictwo CZELEJ Sp.z o.o; 2003.
  • Malek N, Baker MR, Mann C, et al. Electroencepalographic markers in dementia. Acta Neurol Scand. 2017;135(4):388-393. doi:10.1111/ane.12638. PMID:27430350.
  • Mente KP, O'Donnell JK, Jones SE, et al. Fluorodeoxyglucose positron emission tomography (FDG-PET) correlation of histopathology and MRI in prion diseases. Alzheimer Dis Assoc Disord. 2017;31(1):1-7. doi:10.1097/WAD.0000000000000188. PMID:28121634.
  • Parchi P, Castellani R, Capellari S, et al. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Ann Neurol. 1996;39(6):767-78. doi:10.1002/ana.410390613. PMID:8651649.

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