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Article

Atypical sporadic CJD-MM phenotype with white matter kuru plaques associated with intranuclear inclusion body and argyrophilic grain disease.

Neuropathology : official journal of the Japanese Society of Neuropathology - 1 Aug 2015

Berghoff Anna S, Trummert Anita, Unterberger Ursula, Ströbel Thomas, Hortobágyi Tibor, Kovacs Gabor G

Abstract excerpt

We describe an atypical neuropathological phenotype of sporadic Creutzfeldt-Jakob disease in a 76-year-old man. The clinical symptoms were characterized by progressive dementia, gait ataxia, rigidity and urinary incontinence. The disease duration was 6 weeks. MRI did not show prominent atrophy or hyperintensities in cortical areas, striatum or thalamus. Biomarker examination of the cerebrospinal fluid deviated...

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Identifiers

PMID: 25783686
DOI: 10.1111/neup.12192

Genes

PRNP

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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