Young-onset CJD: Age and disease phenotype in variant and sporadic forms

Manuel Corato, Cristina Cereda, Emanuela Cova, Carlo Ferrarese, Mauro Ceroni

Research output: Contribution to journalArticlepeer-review

Abstract

Since 1996, there have been over 140 reports of a Creutzfeldt-Jakob disease variant (vCJD), with a striking prevalence of these cases in the UK. The main peculiarity of vCJD is its onset in young people, but other features also distinguish it from sporadic CJD. Despite epidemiological data suggesting a link with bovine spongiform encephalopathy, the origin of vCJD is not completely understood. We hypothesized that the onset of vCJD at a young age might contribute to the disease phenotype. We searched the Medline/PubMed database for all case reports of CJD in the under-30s and selected 20 sporadic CJD patients with a median age at onset of 25.5 years. Our series displays a long disease duration and other vCJD-like features, suggesting that CJD in young people is different from classic CJD and that the vCJD phenotype may be partly related to young age.

Original languageEnglish
Pages (from-to)211-215
Number of pages5
JournalFunctional Neurology
Volume21
Issue number4
Publication statusPublished - Oct 2006

Keywords

  • CJD
  • Sporadic CJD
  • Survival
  • Variant CJD
  • Young

ASJC Scopus subject areas

  • Clinical Neurology
  • Neuroscience(all)

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