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Article

Myoclonus-dystonia syndrome.

Handbook of clinical neurology - 1 Jan 2011

Nardocci Nardo

Abstract excerpt

Myoclonus dystonia syndrome (MDS) refers to a group of heterogeneous nondegenerative clinical conditions characterized by the association of myoclonus and dystonia as the only or prominent symptom. The "core" of MDS is represented by inherited myoclonus-dystonia (M-D), a disorder with autosomal-dominant inheritance and reduced penetrance, beginning in early childhood with a relatively benign course, with...

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Identifiers

PMID: 21496608
DOI: 10.1016/B978-0-444-52014-2.00041-0

Genes

SGCE

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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