Pharmacology of blepharospasm-oromandibular dystonia syndrome

Daniel E. Casey

Research output: Contribution to journalArticlepeer-review

51 Scopus citations

Abstract

Blepharospasm and oromandibular dystonia are clinically similar to other hyperkinetic movement disorders. Dopaminergic antagonist (neuroleptic) and purported cholinergic agonist (deanol) treatment improved symptoms, whereas dopaminergic agonist (carbidopa/levodopa) and cholinergic antagonist (benztropine) drugs worsened symptoms in two patients. This suggested that the syndrome is also pharmacologically related to the hyperkinetic dyskinesias. Symptoms worsened substantially during carbidopa/levodopa but temporarily resolved in one patient and improved in another when the drug was discontinued. This suggests that the pathophysiology of these symptoms involves an idiopathic form of receptor hypersensitivity that can be modified by agonist treatment. The effect of cholinergic agents was less than the effect of dopaminergic drugs, implying that dopamine plays a predominant role in the pathophysiology.

Original languageEnglish (US)
Pages (from-to)690-695
Number of pages6
JournalNeurology
Volume30
Issue number7
DOIs
StatePublished - Jul 1980
Externally publishedYes

ASJC Scopus subject areas

  • Clinical Neurology

Fingerprint

Dive into the research topics of 'Pharmacology of blepharospasm-oromandibular dystonia syndrome'. Together they form a unique fingerprint.

Cite this