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Article

Paroxysmal movement disorders in severe myoclonic epilepsy in infancy.

Brain & development - 1 Sept 2003

Ohtsuka Yoko, Ohmori Iori, Ogino Tatsuya, Ouchida Mamoru, Shimizu Kenji, Oka Eiji

Abstract excerpt

We report on the electroclinical findings and the results of a molecular genetic study of a patient with typical severe myoclonic epilepsy in infancy (TSME) and three with borderline SME (BSME) who showed paroxysmal movement disorders, such as choreoathetosis, dystonia and ballismus, during their...

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Identifiers

PMID: 12907273
DOI: 10.1016/s0387-7604(03)00025-1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12907273-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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