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Article

Sporadic corticobasal syndrome with progranulin mutation presenting as progressive apraxic agraphia.

Archives of neurology - 1 Mar 2011

Passov Victoria, Gavrilova Ralitza H, Strand Edythe, Cerhan Jane H, Josephs Keith A

Abstract excerpt

OBJECTIVE: To examine the relationship between progranulin gene mutation and apraxic agraphia. DESIGN: Case report. SETTING: Tertiary care medical center. PATIENT: A 49-year-old right-handed woman who presented with apraxic agraphia that progressed into the corticobasal syndrome. RESULTS: This woman had no family history of neurodegenerative disease. Magnetic resonance imaging and fluorodeoxyglucose positron...

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PMID: 21403024
DOI: 10.1001/archneurol.2011.26

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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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