Paroxysmal myoclonic dystonia with vocalisations: New entity or variant of preexisting syndromes?

T. E. Feinberg, A. K. Shapiro, E. Shapiro

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

From among 1377 patients with movement disorders, four patients had an unusual movement disorder characterised by paroxysmal bursts of involuntary, regular, repetitive, rhythmic, bilateral, coordinated, simultaneous, stereotypic myoclonus and vocalisations, often associated with tonic symptoms, interference with voluntary functioning, presence of hyperactivity, attention and learning disabilities, and resistance to treatment with haloperidol and other drugs. This symptom complex may represent a new disease entity, referred to here as paroxysmal myoclonal dystonia with vocalisations or a variant or combination of other movement disorders such as Gilles de la Tourette, myoclonic, or dystonic syndromes.

Original languageEnglish
Pages (from-to)52-57
Number of pages6
JournalJournal of Neurology, Neurosurgery and Psychiatry
Volume49
Issue number1
DOIs
StatePublished - 1986

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