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Article

A patient with posterior cortical atrophy possesses a novel mutation in the presenilin 1 gene.

PloS one - 1 Jan 2013

Sitek Emilia J, Narożańska Ewa, Pepłońska Beata, Filipek Sławomir, Barczak Anna, Styczyńska Maria, Mlynarczyk Krzysztof, Brockhuis Bogna, Portelius Erik, Religa Dorota, Barcikowska Maria, Sławek Jarosław, Żekanowski Cezary

Abstract excerpt

Posterior cortical atrophy is a dementia syndrome with symptoms of cortical visual dysfunction, associated with amyloid plaques and neurofibrillary tangles predominantly affecting visual association cortex. Most patients diagnosed with posterior cortical atrophy will finally develop a typical Alzheimer's disease. However, there are a variety of neuropathological processes, which could lead towards a clinical...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 23593396
DOI: 10.1371/journal.pone.0061074
PMCID: PMC3625161

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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