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Research article summary (published 30 Dec 1982):

Recent advances in Gilles de la Tourette syndrome: implications for clinical practice and future research.

Full Abstract

The clinical presentation and natural history of Gilles de la Tourette syndrome (TS) are reviewed. The waxing and waning of symptoms, the rostrocaudal progression of areas of motor involvement, complex stereotypies, and the familial aggregation of TS and chronic multiple tics are suggestions of underlying neurochemical disturbance; whereas attentional problems, impulsivity and obsessive-compulsive behaviors create interesting links with other disorders. The most robust metabolic findings are the lowered CSF HVA in many TS patients, and the positive response of symptoms to dopamine blockers and clonidine particularly, which would be consistent with dopamine receptor hypersensitivity and possible noradrenergic-dopaminergic interactions in TS. However, no definitive account of patho-physiology or genetic contributions to the disorder is yet available.

 

Author information

Author/s: Leckman, J F (JF); Cohen, D J (DJ);

Grants: HD-03008 (Agency:NICHD NIH HHS) ; MH 30929 (Agency:NIMH NIH HHS)

Journal and publication information

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review

Journal: Psychiatric developments (Psychiatr Dev), published in ENGLAND. (Language: eng)

Reference: 1983-; vol 1 (issue 3) : pp 301-16

Dates: Created 1984/05/11; Completed 1984/05/11; Revised 2007/11/14;

PMID: 6324164, status: MEDLINE (last retrieved date: 2/18/2009)

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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MeSH headings (categories)

This article was linked to the MeSH Headings (categories) shown below.

Note: Bold headings indicate primary MeSH headings or qualifiers.

Associated Chemicals: Parasympathomimetics (0) ; Receptors, Adrenergic (0) ; Homovanillic Acid (306-08-1) ; Clonidine (4205-90-7) ; Serotonin (50-67-9) ; Dopamine (51-61-6) ; Haloperidol (52-86-8) ; Physostigmine (57-47-6)

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