At the back of the mind of a layperson as well as those in the medical profession, a youngster
who tics and swears is immediately tagged with the title of Tourette Syndrome (TS). This sort-of
reflex association may turn out to be correct in some youngsters, however, this youngster may have
tics due to other conditions rather than Tourette syndrome. Moreover, children (and adults) without
TS often swear or use obscene phrases as youngster do nowadays. During the last 50 years, it became
evident that TS is a unique chronic neuropsychiatric complex disorder with early childhood onset
and an evolving course which is often characterized by additional comorbidities such as Attention
Deficit Hyperactivity Disorder (ADHD) and Obsessive-Compulsive Disorder (OCD), a combination
suggesting a possible involvement of the corpus striatum outflow tracts. Indeed, the beneficial effect
of Haloperidol, a dopamine D2 receptor antagonist first synthetized by Bert Hermans at the Janssen
Pharmaceutica in 1958 [1], and the successful trial of this newly introduced butyrophenone in several patients with TS in 1961
[2, 3], laid the basis for extensive research on the pathophysiology of the syndrome which with the advanced modern functional
neuroimaging extended our knowledge on the close link between certain neuro-functional circuits, movements and behaviors.
Interestingly, the emphasis on tics and their rich repertoire is the rule in many publications dedicated to the syndrome, while
the behavioral and psychiatric features are frequently “neglected “. Tics are also the main issue discussed in recent publications
dedicated to the pathophysiology of TS, while quite rare publications dealt in-depth with sleep abnormalities frequently
experienced by the patients.
It is obvious that for successful therapeutic intervention(s), it is crucial that the treating team will include specialists for each
of the "many faces” of the syndrome. For the readers of this journal, the main field of interest of which is therapeutics, the
present thematic mini issue of Current Drug Therapy authored by multidisciplinary experts on TS provides a short clinical
description of the back-bone of TS symptomatology, and detailed up-to-date reviews of the neurophysiology, and sleep
characteristics of the syndrome. Familiarity with the “many faces” of the syndrome is necessary for sound therapeutic
considerations, therefore, the last chapter is dedicated to past and present drug therapy for TS.
We believe that this multidisciplinary format dedicated to TS will help in developing the concept that successful treatment
of tics is not enough because tics may have a lesser impact on the quality of life than the associated comorbidities. Since
comorbidities may not be evident when tics appear at a relatively young age, those should be evaluated routinely and treated
timely by a multidisciplinary team.