Literature DB >> 373455

Creutzfeldt-Jakob disease and optic atrophy.

R L Lesser, D M Albert, A R Bobowick, F H O'Brien.   

Abstract

A 49-year-old man developed ataxia, myoclonic jerks, cortical blindness, and dementia. In 3 1/2 months, he rapidly deteriorated and died. Clinical and autopsy diagnosis confirmed Creutzfeldt-Jakob disease. The eyes were examined and bilateral optic atrophy was noted. No other ocular changes were noted. Optic atrophy had not been noted before death.

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Year:  1979        PMID: 373455     DOI: 10.1016/0002-9394(79)90070-9

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  4 in total

1.  Electrophysiological and pathological studies on Creutzfeldt-Jakob disease with retinal involvement.

Authors:  J Tsutsui; S Kawashima; I Kajikawa; T Shirabe; A Terao
Journal:  Doc Ophthalmol       Date:  1986-06-16       Impact factor: 2.379

2.  The toxicity of the PrP106-126 prion peptide on cultured photoreceptors correlates with the prion protein distribution in the mammalian and human retina.

Authors:  Jie Gong; Abdeljelil Jellali; Valérie Forster; Jérôme Mutterer; Elisabeth Dubus; Wilko D Altrock; José A Sahel; Alvaro Rendon; Serge Picaud
Journal:  Am J Pathol       Date:  2007-04       Impact factor: 4.307

3.  Creutzfeldt-Jakob disease: a case with extensive white matter degeneration and optic atrophy.

Authors:  Y Kitagawa; F Gotoh; A Koto; S Ebihara; H Okayasu; T Ishii; H Matsuyama
Journal:  J Neurol       Date:  1983       Impact factor: 4.849

Review 4.  Differential Accumulation of Misfolded Prion Strains in Natural Hosts of Prion Diseases.

Authors:  Zoe J Lambert; Justin J Greenlee; Eric D Cassmann; M Heather West Greenlee
Journal:  Viruses       Date:  2021-12-07       Impact factor: 5.048

  4 in total

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