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Article

Presymptomatic generalized brain atrophy in frontotemporal dementia caused by CHMP2B mutation.

Dementia and geriatric cognitive disorders - 1 Jan 2009

Rohrer Jonathan D, Ahsan R Laila, Isaacs Adrian M, Nielsen Jorgen E, Ostergaard Leif, Scahill Rachael, Warren Jason D, Rossor Martin N, Fox Nick C, Johannsen Peter

Abstract excerpt

BACKGROUND/AIMS: CHMP2B mutations are a rare cause of familial frontotemporal dementia (FTD). The clinical syndrome is dominated by personality change and behavioural symptoms, but language, memory, calculation and praxis impairments are also seen early in the course of the disease. There are no...

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Identifiers

PMID: 19202337
DOI: 10.1159/000200466

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19202337-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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