Literature DB >> 2250174

Pre-mortem diagnosis of Creutzfeldt-Jakob disease by detection of abnormal cerebrospinal fluid proteins.

K S Blisard1, L E Davis, M G Harrington, J K Lovell, M Kornfeld, M L Berger.   

Abstract

Creutzfeldt-Jakob disease (CJD) may be difficult to diagnose early or when it has an atypical presentation. We describe two patients with progressive dementia in whom the results of diagnostic brain biopsies were unhelpful. Spinal fluid from these patients, analyzed by two-dimensional electrophoresis, contained two abnormal proteins (Nos. 130 and 131, with relative molecular masses of 26,000 and 29,000 daltons and isoelectric points of 5.2 and 5.1). These findings suggested a provisional diagnosis of Creutzfeldt-Jakob disease, which was confirmed in both patients at autopsy. Detection of these abnormal cerebrospinal fluid proteins appears to be a valuable laboratory adjunct in evaluating patients with an unexplained progressive dementia.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2250174     DOI: 10.1016/0022-510x(90)90201-w

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  2 in total

1.  Visual hallucinations: an unusual manifestation of sporadic Creutzfeldt-Jakob disease termed the 'Heidenhain variant'.

Authors:  R Gooriah; B E A Dafalla; S Tun; T C Venugopalan; K K Lwin
Journal:  J Neurol       Date:  2014-10-07       Impact factor: 4.849

Review 2.  Prions and related neurological diseases.

Authors:  M Pocchiari
Journal:  Mol Aspects Med       Date:  1994
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.