Literature DB >> 9038434

Clinical and diagnostic findings in a patient with Creutzfeldt-Jakob disease (type Heidenhain).

W Staffen1, E Trinka, B Iglseder, P Pilz, N Homann, G Ladurner.   

Abstract

A 61-year-old woman had Creutzfeldt-Jakob disease, type Heidenhain, that progressed for 4 months until death, 3 of which she spent in a hospital. The diagnosis was verified by autopsy. Consecutive brain computed tomography, magnetic resonance imaging, blood flow measurements, electroencephalography (EEG), and routine laboratory tests were performed. All imaging techniques showed nonspecific pathological changes, whereas EEG revealed alterations indicative for Creutzfeldt-Jakob disease.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9038434     DOI: 10.1111/jon19977150

Source DB:  PubMed          Journal:  J Neuroimaging        ISSN: 1051-2284            Impact factor:   2.486


  3 in total

1.  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.  Three Cases of Creutzfeldt-Jakob Disease with Visual Disturbances as Initial Manifestation.

Authors:  Toshiro Sakuma; Satoshi Watanabe; Ayumi Ouchi; Yoshihito Sakanishi; Atsushi Mizota; Nobuyuki Ebihara
Journal:  Case Rep Ophthalmol       Date:  2019-10-23

3.  Hypertrophic Olivary Degeneration and Movement Disorder in a Patient with Familial Creutzfeldt-Jakob Disease.

Authors:  Andre Granger; Shashank Agarwal; Andres Andino; Patrick Kwon; Elina Zakin
Journal:  Cureus       Date:  2020-10-08
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.