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Article

Reduction of striatal glucose metabolism in McLeod choreoacanthocytosis.

Journal of neurology, neurosurgery, and psychiatry - 1 Apr 2001

Oechsner M, Buchert R, Beyer W, Danek A

Abstract excerpt

McLeod syndrome is a distinct form of neuroacanthocytosis. Its defining feature is the depression of erythrocyte Kell antigens. The underlying X chromosomal mutations cause a dysfunction of an erythrocyte membrane protein Kx. A choreatic movement disorder with caudate atrophy in CT and MRI has been reported in McLeod syndrome later in the course of the disease. Positron emission tomography with 18F-deoxyglucose...

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Identifiers

PMID: 11254778
DOI: 10.1136/jnnp.70.4.517
PMCID: PMC1737311

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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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