Literature DB >> 22436171

Sporadic Creutzfeldt-Jakob disease: a description of two cases.

Kavita Das1, Rebecca Davis, Brett Dutoit, Brian Parsons.   

Abstract

Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare and devastating illness. It is the most frequently encountered form of the spongiform encephalopathies with 50 new cases a year in the UK. It presents with a myriad of symptoms reflecting central nervous system dysfunction and is characterized by a rapidly progressive dementia leading to death. The disease process can pose multiple challenges: diagnostic conundrums, complexities in management, and palliative care issues. Good coordinated care between services and information is paramount in adequate management and delivery of care for patients suffering from sCJD.Psychiatry services frequently become involved in the assessment and management of sCJD.

Entities:  

Mesh:

Year:  2012        PMID: 22436171     DOI: 10.1017/S1041610212000373

Source DB:  PubMed          Journal:  Int Psychogeriatr        ISSN: 1041-6102            Impact factor:   3.878


  2 in total

1.  Rare V203I mutation in the PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease.

Authors:  Qi Shi; Cao Chen; Xian-Jun Wang; Wei Zhou; Ji-Chun Wang; Bao-Yun Zhang; Chen Gao; Chen Gao; Jun Han; Xiao-Ping Dong
Journal:  Prion       Date:  2013 May-Jun       Impact factor: 3.931

2.  Developing neuropalliative care for sporadic Creutzfeldt-Jakob Disease.

Authors:  Krista L Harrison; Sarah B Garrett; Joni Gilissen; Michael J Terranova; Alissa Bernstein Sideman; Christine S Ritchie; Michael D Geschwind
Journal:  Prion       Date:  2022-12       Impact factor: 3.931

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.