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Young-onset sporadic Creutzfeldt-Jakob disease with atypical phenotypic features: a case report

Young-onset sporadic Creutzfeldt-Jakob disease with atypical phenotypic features: a case report

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_bea8e8d0d36d44e7830862610ad4fb1f

Young-onset sporadic Creutzfeldt-Jakob disease with atypical phenotypic features: a case report

About this item

Full title

Young-onset sporadic Creutzfeldt-Jakob disease with atypical phenotypic features: a case report

Publisher

England: BioMed Central Ltd

Journal title

Journal of medical case reports, 2019-05, Vol.13 (1), p.163-163, Article 163

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Sporadic Creutzfeldt-Jakob disease, with a mean survival of 6 months, is duly considered among the most fatal neurological disorders. Rapidly progressive dementia with multi-axial involvement of the nervous system is the known presentation. Although, the peak age at onset is between sixth and eighth decades, cases of young-onset sporadic Creutzfeld...

Alternative Titles

Full title

Young-onset sporadic Creutzfeldt-Jakob disease with atypical phenotypic features: a case report

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_bea8e8d0d36d44e7830862610ad4fb1f

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_bea8e8d0d36d44e7830862610ad4fb1f

Other Identifiers

ISSN

1752-1947

E-ISSN

1752-1947

DOI

10.1186/s13256-019-2089-5

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