Cortical myoclonus in Huntington's disease.

doi:10.1002/mds.870090609

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Article

Cortical myoclonus in Huntington's disease.

Movement disorders : official journal of the Movement Disorder Society - 1 Nov 1994

Thompson P D, Bhatia K P, Brown P, Davis M B, Pires M, Quinn N P, Luthert P, Honovar M, O'Brien M D, Marsden C D

Abstract excerpt

We describe three patients with Huntington's disease, from two families, in whom myoclonus was the predominant clinical feature. The diagnosis was confirmed at autopsy in two cases and by DNA analysis in all three. These patients all presented before the age of 30 years and were the offspring of...

Topics

Adult
Alleles
Cerebral Cortex
DNA
Electroencephalography
Electromyography
Evoked Potentials, Somatosensory
Female
Humans
Huntington Disease
Male
Myoclonus
Neurologic Examination
Pedigree
Polymerase Chain Reaction
Reflex

Source

Open in PubMed

Identifiers

PMID: 7845404
DOI: 10.1002/mds.870090609

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-7845404-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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