By Dr Barbara Coffey, MD and Maxwell Luber
Tourette syndrome (TS), also known as Tourette’s Disorder, is a neurodevelopmental disorder characterized by multiple motor tics and at least one vocal tic present for greater than one year. Among the neurodevelopmental disorders in the DSM-5, TS is the most complex of the spectrum of tic disorders , which includes:
Persistent motor or vocal tic disorder: one or more motor or vocal tics have been present for greater than one year
Provisional tic disorder: motor and/or vocal tics have been present for less than a year.
Psychiatric disorders, such as obsessive-compulsive disorder (OCD) and attention-deficit hyperactivity disorder (ADHD) frequently co-occur in TS.
 Tic symptoms typically begin in early childhood, peak before puberty, and attenuate later in adolescence. [3, 4]
VIDEO Symptoms and phenomenology
Tics are rapid, repetitive, non-rhythmic movements or vocalizations. Motor and vocal tics are divided into two classes: simple and complex. Simple motor tics are brief movements involving one muscle group. Simple vocal tics are characterized by simple sounds.
Simple motor tics include eye blinks, facial grimaces, head and neck jerks, and shoulder shrugs. Briefly sustained postures (e.g., blepharospasm, oculogyric movements, and sustained mouth opening) can also be classified as simple motor tics.
Simple vocal tics include coughing, sniffing, throat clearing, grunting, and squeaking.
Complex motor tics are more purposeful or orchestrated patterns of movement; complex vocal tics are longer, more orchestrated patterns of speech.
Examples of complex motor tics are turning while walking, echopraxia (imitating gestures) and copropraxia (obscene gestures).
Complex vocal tics include repeated words or phrases, echolalia (repeating another person's words or phrases) and coprolalia (uttering obscenities).
 Although coprolalia can cause considerable social distress, it is infrequent, and occurs in only approximately 10% of patients. 
A distinguishing characteristic of tics are the sensations that may precede the movement or sound, termed premonitory sensations or "urges." Sometimes patients can localize these feelings to particular parts of the body from which the tic emerged.
Even if not localizable, patients often describe a feeling of inner discomfort, using words such as a “build up of tension," or describe an unexplainable urge or impulse to perform the tic. Most patients experience an intensification of these sensations or urges when they suppress their tics.
Patients also often describe a strong need to repeat the tic until it feels "just right". After performing the tic, a sense of relief is experienced, although sometimes brief.
Descriptions of these sensations may be difficult for younger patients to express, but there is a quantitative, pictorial rating scale of these urges that can be used with children. [
TS is reported worldwide, with estimated prevalence from 0.3% to 0.9%. [
7]   It affects boys 3 to 4 times more frequently than girls.  The vast majority of individuals with TS have behavioral and/or emotional symptoms or disorders; only 12% across all ages are reported to have only tics without other associated conditions. 
From a worldwide dataset, ADHD is the most common comorbid psychiatric disorder, and accounts for about 55% of the behavioral findings.
 Other disorders, such as mood and anxiety disorders and learning disorders, are also frequently present.  Etiology
The cause of TS remains unknown, although evidence from genetic studies suggests that TS is inherited.
 Genetic factors seem to be the most important etiology, given significant familial aggregation and supporting twin studies.  
Monozygotic twin studies show 53% concordance for TS and 77% for persistent (chronic) motor tics, whereas dizygotic twins show 8% and 23% concordance, respectively.
Environmental factors, including perinatal insults, sex-hormone exposure during brain development, and psychosocial stressors, are also thought to contribute, and thus the overall expression of TS is thought to be multifactorial.
  Diagnosis
Diagnosis is made by a comprehensive clinical history from reliable sources, most often parents. Currently there is no identifiable biological marker for a TS diagnosis. A thorough, detailed history focusing on onset, time course, phenomenology such as urges or sensations, exacerbating and ameliorating factors, family history, and comorbid symptoms is essential. A general medical and neurological exam is indicated.
When eliciting history from the parent and patient, inquiry regarding onset of tics is important, as they typically begin in early childhood, followed by a waxing and waning course.
 Often tics worsen in late childhood prior to puberty. 
Although tics tend to wax and wane, with one tic replacing another, sometimes tics can present abruptly or in acute bursts. Explosive, acute onset over 24 to 48 hours, particularly of OCD symptoms, may be suggestive of infectious or autoimmune etiology.
  
Potential day-to-day exacerbating factors, such as medications (stimulants in some patients, including caffeine and over-the-counter decongestants or cold remedies), fatigue, boredom, and stressors should be noted.
Tic symptoms may be difficult to disentangle from other common childhood symptoms of allergies or cough-variant asthma. Inquiry regarding seasonal patterns, and presence of other allergy-associated symptoms such as rhinitis and post-nasal drip, can be helpful in the differential diagnostic process.
Additionally, at times it may be difficult to differentiate complex motor tics from compulsions, as OCD symptoms frequently co-occur in children with TS. Repetitive behaviors preceded by urges or sensations are more likely to be complex tics, whereas repetitive behaviors that are preceded by a cognition, often a worry, are more likely to be compulsions.
For information on the latest treatment options, please visit the Tourette Association of America's
treatment page. Further Reading
For more information on Tourette's syndrome, please visit
Touette.org About Barbara Coffey
Barbara Coffey, M.D., M.S., is an internationally known specialist in tics and Tourette’s Disorder and related problems. She is Professor in the Department of Psychiatry and Director of the Tics and Tourette’s Disorder Clinical and Research Program at the Icahn School of Medicine at Mt. Sinai. (ISMMS).
Prior to her move to ISMMS, Dr. Coffey was Associate Professor in the Department of Child and Adolescent Psychiatry at the NYU School of Medicine, and Director of the Tics and Tourette’s Clinical and Research Program at the NYU Child Study Center.
Dr. Coffey received her B.A. in Biology and Psychology from the University of Rochester, her M.D. from Tufts University School of Medicine and her M.S. in Epidemiology from the Harvard School of Public Health.
She completed a residency in general psychiatry at Boston University Hospital and a residency in child and adolescent psychiatry at the Tufts University School of Medicine.
Dr. Coffey held past positions as Director of Pediatric Psychopharmacology at McLean Hospital and Director of the Tourette's Clinics at McLean and Massachusetts General Hospitals in Boston between 1992 and 2001, and remained on the faculty of the Harvard Medical School as a Clinical Associate at Massachusetts General Hospital until January 2007. Dr. Coffey has repeatedly been recognized by America’s Best Doctors, Boston’s Best Doctors, and New York’s Best Doctors.
Dr. Coffey served on the Committee on Written Examination in Child and Adolescent Psychiatry and the Steering Committee on Certification in Child and Adolescent Psychiatry for the American Board of Psychiatry and Neurology.
Author of more than 100 publications in peer reviewed journals, book chapters, and texts, Dr. Coffey has served as an Associate Editor of the
Journal of Child and Adolescent Psychopharmacology. Her research interests have focused on the phenomenology, comorbidity, neurobiology and treatment of Tourette’s Disorder and related problems. About Maxwell Luber
Maxwell Luber, B.A., is a Clinical Research Coordinator of the Tics and Tourette’s Clinical and Research Program at the Icahn School of Medicine at Mt. Sinai. Maxwell Luber received his B.A. in Psychology from Temple University.
American Psychiatric Association. Diagnostic and statistical manual of mental disorders, 5th ed., (DSM-5). Washington, DC: American Psychiatric Publishing; 2013.
Fahn S, Jankovic J, Hallet M, et al. Chapter 17: Tics and Tourette syndrome. In: Principles and practice of movement disorders. Philadelphia, PA: Churchill Livingstone Elsevier; 2007:409-422.
Leckman JF, Zhang H, Vitale A, et al. Course of tic severity in Tourette syndrome: the first two decades. Pediatrics. 1998;102:14-19. [Abstract]
http://www.ncbi.nlm.nih.gov/pubmed/9651407 Bloch MH, Peterson BS, Scahill L, et al. Adulthood outcome of tic and obsessive-compulsive symptom severity in children with Tourette syndrome. Arch Pediatr Adolesc Med. 2006;160:65-69.[Abstract]
http://www.ncbi.nlm.nih.gov/pubmed/16389213 [Full Text] http://archpedi.ama-assn.org/cgi/content/full/160/1/65 Singer HS. Tourette's syndrome: from behaviour to biology. Lancet Neurol. 2005;4:149-159. [Abstract]
http://www.ncbi.nlm.nih.gov/pubmed/15721825 Woods DW, Piacentini J, Himle MB, Chang S. Premonitory Urge for Tics Scale (PUTS): initial psychometric results and examination of the premonitory urge phenomenon in youths with Tic disorders. J Dev Behav Pediatr. 2005;26(6):397-403.[Abstract]
https://www.ncbi.nlm.nih.gov/pubmed/16344654 Scharf, J. M., Miller, L. L., Gauvin, C. A., Alabiso, J., Mathews, C. A., & Ben-Shlomo, Y. (2015). Population prevalence of Tourette syndrome: a systematic review and meta-analysis. Mov Disord, 30(2), 221-228. doi: 10.1002/mds.26089
Tanner CM, Goldman SM. Epidemiology of Tourette syndrome. Neurol Clin. 1997;15:395-402.[Abstract]
http://www.ncbi.nlm.nih.gov/pubmed/9115469 Comings DE, Comings BG. Tourette syndrome: clinical and psychological aspects of 250 cases. Am J Hum Genet. 1985;37:435-450. [Abstract]
http://www.ncbi.nlm.nih.gov/pubmed/3859204 Tanner C. Epidemiology. In: Kurlan R, ed. Handbook of Tourette's syndrome and associated tic and behavioral disorders. New York, NY: Marcel Dekker; 2004:399-410.
Freeman RD, Fast DK, Burd L, et al. An international perspective on Tourette syndrome: selected findings from 3,500 individuals in 22 countries. Dev Med Child Neurol. 2000;42:436-447.[Abstract]
http://www.ncbi.nlm.nih.gov/pubmed/10972415 Freeman RD; Tourette Syndrome International DatabaseConsortium. Tic disorders and ADHD: answers from a world-wide clinical dataset on Tourette syndrome. Eur Child Adolesc Psychiatry. 2007;16(suppl 1):15S-23S. [Abstract]
http://www.ncbi.nlm.nih.gov/pubmed/17665279 Hirschtritt ME, Lee PC, Pauls DL, et al. Lifetime prevalence, age of risk, and genetic relationships of comorbid psychiatric disorders in Tourette syndrome. JAMA Psychiatry. 2015;72(4):325-33 [Abstract]
https://www.ncbi.nlm.nih.gov/pubmed/25671412 Pauls DL, Cohen DJ, Heimbuch R. Familial pattern and transmission of Gilles de la Tourette syndrome and multiple tics. Arch Gen Psychiatry. 1981;38:1091-1093. [Abstract]
http://www.ncbi.nlm.nih.gov/pubmed/6945827 Keen-Kim D, Freimer NB. Genetics and epidemiology of Tourette syndrome. J Child Neurol. 2006;21:665-671. [Abstract]
http://www.ncbi.nlm.nih.gov/pubmed/16970867 Mataix-Cols, D., Isomura, K., Perez-Vigil, A., Chang, Z., Ruck, C., Larsson, K. J., Lichtenstein, P. (2015). Familial Risks of Tourette Syndrome and Chronic Tic Disorders. A Population-Based Cohort Study. JAMA Psychiatry, 72(8), 787-793. doi: 10.1001/jamapsychiatry.2015.0627
Price RA, Kidd KK, Cohen DJ, et al. A twin study of Tourette syndrome. Arch Gen Psychiatry. 1985;42:815-820. [Abstract]
http://www.ncbi.nlm.nih.gov/pubmed/3860194 Swain JE, Scahill L, Lombroso PJ, et al. Tourette syndrome and tic disorders: a decade of progress. J Am Acad Child Adolesc Psychiatry. 2007;46:947-968. [Abstract]
http://www.ncbi.nlm.nih.gov/pubmed/17667475 Woods DW, Piacentini J, Himle MB, et al. Premonitory Urge for Tics Scale (PUTS): initial psychometric results and examination of the premonitory urge phenomenon in youths with tic disorders. J Dev Behav Pediatr. 2005;26:397-403. [Abstract]
http://www.ncbi.nlm.nih.gov/pubmed/16344654 Chang K, Frankovich J, Cooperstock M, et al. Clinical evaluation of youth with pediatric acute-onset neuropsychiatric syndrome (PANS): recommendations from the 2013 PANS Consensus Conference. J Child Adolesc Psychopharmacol. 2015;25:3-13. [Abstract]
http://www.ncbi.nlm.nih.gov/pubmed/25325534 [Full Text] http://online.liebertpub.com/doi/pdf/10.1089/cap.2014.0084 Frankovich J, Thienemann M, Pearlstein J, et al. Multidisciplinary clinic dedicated to treating youth with pediatric acute-onset neuropsychiatric syndrome: presenting characteristics of the first 47 consecutive patients. J Child Adolesc Psychopharmacol. 2015;25:38-47. [Abstract]
http://www.ncbi.nlm.nih.gov/pubmed/25695943 Murphy TK, Patel PD, McGuire JF, et al. Characterization of the pediatric acute-onset neuropsychiatric syndrome phenotype. J Child Adolesc Psychopharmacol. 2015;25:14-25. [Abstract]
http://www.ncbi.nlm.nih.gov/pubmed/25314221 Conelea, C. A., & Woods, D. W. (2008). The influence of contextual factors on tic expression in Tourette's syndrome: a review. J Psychosom Res, 65(5), 487-496. doi: 10.1016/j.jpsychores.2008.04.010
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