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Article

Chorea-acanthocytosis genotype in the original critchley kentucky neuroacanthocytosis kindred.

Archives of neurology - 1 Oct 2011

Velayos-Baeza Antonio, Holinski-Feder Elke, Neitzel Birgit, Bader Benedikt, Critchley Edmund M R, Monaco Anthony P, Danek Adrian, Walker Ruth H

Abstract excerpt

OBJECTIVE: To determine the molecular nature of the neurological disease in the seminal family reported by Critchley et al in the 1960s, characterized by a hyperkinetic movement disorder and the appearance of acanthocytosis on peripheral blood smear. The eponym Levine-Critchley syndrome, subsequently termed neuroacanthocytosis, has been applied to symptomatically similar, but genetically distinct, disorders,...

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Identifiers

PMID: 21987550
DOI: 10.1001/archneurol.2011.239
PMCID: PMC4615612

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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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