Abstract
Gilles de la Tourette’s syndrome (TS) is a chronic, familial neuropsychiatric disorder of unknown etiology characterized by motor and phonic tics that vary in severity and form and a range of complex behavior problems, including some forms of obsessive compulsive disorder (OCD). Although its etiology remains unknown, the vertical transmission of TS within families follows a pattern consistent with an autosomal dominant form of inheritance.1 2 For nearly a century following its original description in 1885, TS was regarded as a rare medical curiosity. It received relatively little attention until the late 1960s, when interest was renewed largely as a result of the finding that approximately 80% of patients responded well clinically to treatment with haloperidol, a dopamine receptor blocking agent.3 4 Subsequent expanded research efforts have led to several notable interrelated advances: (1) a greater understanding of the range of phenotypic expression and the possible significance of comorbid conditions, (2) a realization that TS and related conditions are much more common than had previously been considered, (3) a better understanding of the familial transmission of the syndrome, and (4) an emerging body of neurobiologic and pharmacological data concerning the pathophysiology and neuropathological correlates of TS.
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Chappell, P.B., Leckman, J.F., Pauls, D., Cohen, D.J. (1990). Biochemical and Genetic Studies of Tourette’s Syndrome. In: Deutsch, S.I., Weizman, A., Weizman, R. (eds) Application of Basic Neuroscience to Child Psychiatry. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-0525-5_15
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