| Literature DB >> 21168060 |
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.Entities:
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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