Early sensory disturbances and seizures are common manifestations of familial Creutzfeldt-Jakob disease due to E200K PRNP mutation: Case report from two Peruvian families
Author:
Funder
Fogarty International Center
Publisher
Elsevier BV
Subject
Clinical Neurology,General Medicine,Surgery
Reference10 articles.
1. Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease;Lee;Am. J. Hum. Genet.,1999
2. Genetic prion disease: experience of a rapidly progressive dementia center in the United States and a review of the literature;Takada;Am. J. Med. Genet. Part B Neuropsychiatr. Genet. Off. Publ. Int. Soc. Psychiatr. Genet.,2017
3. Prion-specific and surrogate CSF biomarkers in Creutzfeldt-Jakob disease: diagnostic accuracy in relation to molecular subtypes and analysis of neuropathological correlates of p-tau and Aβ42 levels;Lattanzio;Acta Neuropathol. (Berl.),2017
4. Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation;Chapman;J. Neurol. Neurosurg. Psychiatry,1993
5. Clinical aspects of common genetic Creutzfeldt-Jakob disease;Schelzke;Eur. J. Epidemiol.,2012
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