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Article

Deep brain stimulation in myoclonus-dystonia syndrome.

Movement disorders : official journal of the Movement Disorder Society - 1 Jun 2004

Cif Laura, Valente Enza Maria, Hemm Simone, Coubes Christine, Vayssiere Nathalie, Serrat Stéphanie, Di Giorgio Annalisa, Coubes Philippe

Abstract excerpt

Myoclonus-dystonia syndrome (MDS) is an autosomal dominant disorder characterized by bilateral myoclonic jerks. An 8-year-old boy presenting with early onset, medically intractable, MDS due to a mutation in the epsilon-sarcoglycan gene (SGCE) underwent chronic bilateral stimulation of the globus pallidus internus, which eliminates both myoclonus and dystonia. We conclude that deep brain stimulation can be an...

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Source

Identifiers

PMID: 15197720
DOI: 10.1002/mds.20030

Genes

SGCE

Provenance

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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