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Article
August 1983

Neuroanatomy of Gilles de la Tourette's Syndrome Possible Midbrain Involvement

Author Affiliations

From the Department of Neurology, Beth Israel Hospital, and Harvard Medical School, Boston. Dr Devinsky is now with the Department of Neurology, New York Hospital-Cornell Medical Center.

Arch Neurol. 1983;40(8):508-514. doi:10.1001/archneur.1983.04210070048013
Abstract

• Alterations of the dopaminergic system are well documented in Gilles de la Tourette's syndrome (TS). Dopamine (DA)—receptor blockers often relieve symptoms, whereas DA agonists acutely exacerbate them. The cluster of symptoms and known localization of lesions in encephalitis lethargica (EL), together with studies on the anatomy of vocalization, suggest that damage to the periaqueductal gray and midbrain tegmentum may be involved in TS. Pharmacologic findings in patients with TS and EL suggest that oculogyric crises and obsessions are associated with diminished DA levels and the development of supersensitive DA receptors, and that tics occur when these receptors are stimulated.

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