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Article

Alternating hemiplegia of childhood in Denmark: clinical manifestations and ATP1A3 mutation status.

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society - 1 Jan 2014

Hoei-Hansen Christina E, Dali Christine Í, Lyngbye Troels J B, Duno Morten, Uldall Peter

Abstract excerpt

Alternating hemiplegia of childhood (AHC) is a rare neurodevelopmental disorder characterized by early-onset recurrent distinctive hemiplegic episodes commonly accompanied by other paroxysmal features and developmental impairment. De novo mutations in ATP1A3 were recently identified as a genetic cause of AHC. To describe the entire Danish cohort of paediatric AHC patients we approached neuropaediatricians...

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Identifiers

PMID: 24100174
DOI: 10.1016/j.ejpn.2013.08.007

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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