Literature DB >> 21168060

[Creutzfeldt - Jakob presenting with isolated visual symptoms: the Heidenhain variant].

I del Barrio-Manso1, A Toribio-García, M Cordero-Coma, L Tuñón, E Baragaño.   

Abstract

CLINICAL CASE: We report the case of a 67 year old female complaining of decreased vision and diagnosed with the Heidenhain variant of sporadic Creutzfeldt-Jakob disease. Her past medical history was unremarkable. She died less than three months after the onset. DISCUSSION: The Heidenhain variant of sporadic Creutfeld-Jakob disease should be suspected in patients suffering from early visual disturbances, unremarkable ophthalmic examination, and subsequent rapid decline of their cognitive function. A complete neurological exam including electroencephalogram recordings and magnetic resonance is mandatory. These patients share a common genotype (PRNP codon 129 MM) associated with a clinically typical disease course.
Copyright © 2010 Sociedad Española de Oftalmología. Published by Elsevier Espana. All rights reserved.

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Year:  2010        PMID: 21168060     DOI: 10.1016/j.oftal.2010.09.014

Source DB:  PubMed          Journal:  Arch Soc Esp Oftalmol        ISSN: 0365-6691


  2 in total

Review 1.  Neuroradiology of human prion diseases, diagnosis and differential diagnosis.

Authors:  Simona Gaudino; Emma Gangemi; Raffaella Colantonio; Annibale Botto; Emanuela Ruberto; Rosalinda Calandrelli; Matia Martucci; Maria Gabriella Vita; Carlo Masullo; Alfonso Cerase; Cesare Colosimo
Journal:  Radiol Med       Date:  2017-01-21       Impact factor: 3.469

2.  Revisiting the Heidenhain Variant of Creutzfeldt-Jakob Disease: Evidence for Prion Type Variability Influencing Clinical Course and Laboratory Findings.

Authors:  Simone Baiardi; Sabina Capellari; Anna Ladogana; Silvia Strumia; Mario Santangelo; Maurizio Pocchiari; Piero Parchi
Journal:  J Alzheimers Dis       Date:  2016       Impact factor: 4.472

  2 in total

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