Tourette Syndrome: Training for Law Enforcement
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Tourette's Syndrome
Tourette’s Syndrome CHRISTOPHER KENNEY, MD; SHENG-HAN KUO, MD; and JOOHI JIMENEZ-SHAHED, MD Baylor College of Medicine, Houston, Texas Tourette’s syndrome is a movement disorder most commonly seen in school-age children. The incidence peaks around preadolescence with one half of cases resolving in early adult- hood. Tourette’s syndrome is the most common cause of tics, which are involuntary or semi- voluntary, sudden, brief, intermittent, repetitive movements (motor tics) or sounds (phonic tics). It is often associated with psychiatric comorbidities, mainly attention-deficit/hyperac- tivity disorder and obsessive-compulsive disorder. Given its diverse presentation, Tourette’s syndrome can mimic many hyperkinetic disorders, making the diagnosis challenging at times. The etiology of this syndrome is thought to be related to basal ganglia dysfunction. Treatment can be behavioral, pharmacologic, or surgical, and is dictated by the most incapacitating symp- toms. Alpha2-adrenergic agonists are the first line of pharmacologic therapy, but dopamine- receptor–blocking drugs are required for multiple, complex tics. Dopamine-receptor–blocking drugs are associated with potential side effects including sedation, weight gain, acute dystonic reactions, and tardive dyskinesia. Appropriate diagnosis and treatment can substantially improve quality of life and psychosocial functioning in affected children. (Am Fam Physician. 2008;77(5):651-658, 659-660. Copyright © 2008 American Academy of Family Physicians.) ▲ Patient information: n 1885, Georges Gilles de la Tourette normal context or in inappropriate situa- A handout on Tourette’s described the major clinical features tions, thus calling attention to the person syndrome, written by the authors of this article, is of the syndrome that now carries his because of their exaggerated, forceful, and provided on p. -
Did Mozart Suffer from Gilles De La Tourette Syndrome?ଝ
r e v c o l o m b p s i q u i a t . 2 0 1 7;4 6(2):110–115 www.elsevier.es/rcp Epistemology, philosophy of the mind and bioethics Did Mozart suffer from Gilles de la Tourette syndrome?ଝ a,∗ b Leonardo Palacios-Sánchez , Juan Sebastián Botero-Meneses , c d d Laura Daniela Vergara-Méndez , Natalia Pachón , Arianna Martínez , d Santiago Ramírez a Departamento de Neurología, Universidad del Rosario, Bogotá, Colombia b Grupo de Investigación en Neurociencia (NEUROS), Universidad del Rosario, Bogotá, Colombia c Departamento de Pediatría, Universidad del Rosario, Bogotá, Colombia d Semillero de Investigación en Neurociencia, Bogotá, Colombia a r t i c l e i n f o a b s t r a c t Article history: The personal and private lives of great men and women in history, like writers, painters Received 1 April 2016 and musicians, have been the subject of great interest for many years. A clear example Accepted 4 May 2016 of this is the vast scrutiny is cast over the famous composer, Wolfgang Amadeus Mozart. Available online 3 June 2017 What may have started as curiosity, rapidly evolved into extensive research, as the answers about the musician’s legendary talent may lie in the details of his life (his childhood, his Keywords: relationships, his quirks and his mannerisms). It is usually up to historians, anthropologists or philosophers to delve into the pages of old books, trying to grasp answers and clues. Tourette syndrome Movement disorders However, for some time, physicians have sought their own part in solving the puzzle. -
The ICD-10 Classification of Mental and Behavioural Disorders : Clinical Descriptions and Diagnostic Guidelines
ICD-10 ThelCD-10 Classification of Mental and Behavioural Disorders Clinical descriptions and diagnostic guidelines | World Health Organization I Geneva I 1992 Reprinted 1993, 1994, 1995, 1998, 2000, 2002, 2004 WHO Library Cataloguing in Publication Data The ICD-10 classification of mental and behavioural disorders : clinical descriptions and diagnostic guidelines. 1.Mental disorders — classification 2.Mental disorders — diagnosis ISBN 92 4 154422 8 (NLM Classification: WM 15) © World Health Organization 1992 All rights reserved. Publications of the World Health Organization can be obtained from Marketing and Dissemination, World Health Organization, 20 Avenue Appia, 1211 Geneva 27, Switzerland (tel: +41 22 791 2476; fax: +41 22 791 4857; email: [email protected]). Requests for permission to reproduce or translate WHO publications — whether for sale or for noncommercial distribution — should be addressed to Publications, at the above address (fax: +41 22 791 4806; email: [email protected]). The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers' products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. Errors and omissions excepted, the names of proprietary products are distinguished by initial capital letters. -
Tourette Syndrome in Children
Focus | Clinical Tourette syndrome in children Valsamma Eapen, Tim Usherwood UP TO 20% OF CHILDREN exhibit rapid jerky peak severity at the age of approximately movements (motor tics) that are made 10–12 years, and typically improve by without conscious intention as part of a adolescence or thereafter.6 Background Gilles de la Tourette syndrome (GTS), developmental phase that often lasts a few 1 characterised by motor and vocal tics, weeks to months. Similarly, involuntary has a prevalence of approximately 1% sounds, vocalisations or noises (vocal or Clinical features in school-aged children. Commonly phonic tics) such as coughing and even In addition to simple motor and vocal/ encountered comorbidities of GTS brief screams or shouts may be observed in phonic tics, complex tics may be present include attention deficit hyperactivity some children for brief periods of time. Tics (Table 1). Some complex tics – such as disorder (ADHD) and obsessive- lasting for a few weeks to months are known spitting, licking, kissing, etc – may be compulsive behaviour/disorder (OCB/ OCD). Genetic factors play an important as ‘transient tic disorder’. When single misunderstood or misinterpreted and part in the aetiology of GTS, and family or multiple motor or vocal tics – but not a may result in the young person getting members may exhibit tics or related combination of both – have been present in trouble, especially if these tics include disorders such as ADHD, OCB or OCD. for more than one year, the term ‘chronic involuntary and inappropriate obscene tic disorder’ is used. When both (multiple) gesturing (copropraxia) or copying the Objective The aim of this article is to present a motor and (one or more) vocal tics have been movements of other people (echopraxia). -
Practical Child Psychiatry: the Clinician's Guide
Practical Child Psychiatry: The Clinician's Guide Bryan Lask Sharon Taylor Kenneth P Nunn BMJ PUBLISHING GROUP Practical Child Psychiatry: The clinician’s guide This Page Intentionally Left Blank This Page Intentionally Left Blank Practical Child Psychiatry: The clinician’s guide Bryan Lask Professor of Child and Adolescent Psychiatry, St George's Hospital Medical School, University of London, London, UK and Huntercombe Hospital, Maidenhead, UK Sharon Taylor Specialist Registrar in Child Psychiatry, Academic Unit of Child and Adolescent Psychiatry, Imperial College of Science, Technology and Medicine, St Mary’s Campus, London, UK Kenneth P Nunn Professor of Child Psychiatry, University of Newcastle and Director of Inpatient Child Psychiatry, John Hunter Hospital, Newcastle, New South Wales, Australia © BMJ Publishing Group 2003 BMJ Books is an imprint of the BMJ Publishing Group All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted, in any form or by any means, electronic, mechanical, photocopying, recording and/or otherwise, without the prior written permission of the publishers. First published in 2003 by BMJ Books, BMA House, Tavistock Square, London WC1H 9JR www.bmjbooks.com British Library Cataloguing in Publication Data A catalogue record for this book is available from the British Library ISBN 0 7279 1593 2 Typeset by SIVA Math Setters, Chennai, India Printed and bound in Spain by Graphycems, Navarra Contents Preface vii Foreword ix Acknowledgements xiii Section I: A bird’s eye view 1 1. Background 3 2. Assessment 14 Section II: The clinical picture 19 3. Fears and anxieties 21 4. Post-traumatic stress disorder 34 5. -
Neurological Features of Gilles De La Tourette's Syndrome
J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.36.1.1 on 1 February 1973. Downloaded from Journal of Neurology, Neurosurgery, and Psychiatry, 1973, 36, 1-9 Neurological features of Gilles de la Tourette's syndrome RICHARD D. SWEET, GAIL E. SOLOMON, HENRIETTE WAYNE, ELAINE SHAPIRO, AND ARTHUR K. SHAPIRO From the Departments of Neurology and Psychiatry, Cornell University Medical College, New York, New York 10021, U.S.A. SUMMARY Clinical neurological examinations of 22 patients with Gilles de la Tourette's syndrome and written reports of examinations of seven other patients are reported. Half the personally exam- ined patients had minor motor asymmetries in addition to the typical motor and vocal tics found in all the patients. Thirty-six per cent of patients were left handed or ambidextrous. Electroencephalo- grams performed on 17 of the 22 patients showed non-specific abnormalities in 12 of them. These findings suggest that a neurological disorder underlies Tourette's syndrome, but they do not clarify its nature. Protected by copyright. Tics may be defined as brief purposeless move- (Yeh, McNay, and Goldberg, 1969). It has been ments of a body part which occur at random suggested that a dopamine excess may underlie intervals and cannot be suppressed for long Tourette's syndrome (Snyder, Taylor, Coyle, and periods oftime. Wilson (1927) believed they were Meyerhoff, 1970), but the actual anatomical or psychogenic in origin, while others have empha- pathophysiological abnormality which might sized developmental (Balthasar, 1957) or in- cause Tourette's syndrome and be controlled by flammatory disorders (Creak and Guttman, haloperidol is still unknown. -
Tourette Syndrome— Much More Than Tics Moving Beyond Misconceptions to a Diagnosis
Cover article LOWELL HANDLER First of two parts Tourette syndrome— much more than tics Moving beyond misconceptions to a diagnosis By Samuel H. Zinner, MD Far more people have heard of Tourette syndrome than know what it actually looks and sounds like—or how it feels to the person who has it. That’s a major reason the diagnosis of this condition—the most severe tic disorder—is often missed. A change of perception begins with understanding the breadth and variability of symptoms and being aware of comorbidity. ore than a century has passed since the ical figures (including the Roman Emperor Claudius, French neurologist Georges Gilles de la Wolfgang Amadeus Mozart, and 18th century English Tourette first described the condition literary scholar Samuel Johnson) testify to the wide- that bears his name, a name familiar to spread awareness of TS across cultures and time, de- the lay public and health professionals spite (or perhaps because of) its perceived rarity. So it alike. Once considered so rare that neurologists might seems that the medical community trailed the un- Mexpect to witness the disorder perhaps once in their trained community by centuries in recognizing the professional lifetime, Tourette syndrome (TS) is, in syndrome. fact, common enough that virtually all pediatricians From the time of its initial medical description in will have several patients with this condition in their 1885 until the 1960s, medical experts viewed TS as a practice. Yet, despite its name recognition and the psychological disorder, and treatment was customarily number of people it affects, TS often goes undiag- directed toward psychotherapy. -
SESS Website: Factsheet on Tourette Syndrome
Special Education Support Service: Information on Tourette Syndrome Introductory Note: The Special Education Support Service wishes to acknowledge and thank Breeda Quigley, Learning Support Teacher, Co. Mayo, for her input in the compilation of this document. Breeda has completed postgraduate research on Tourette Syndrome. Note: The following is the stated position of the DES with regard to the educational provision to be provided for a child who has special educational needs arising from a specific assessed syndrome. See Circular 08/02 for further information. “The level of additional support to be provided for children who present with a particular syndrome e.g. Down Syndrome, William's Syndrome and Tourette's Syndrome will be determined following consideration of psychological or other specialist reports which details the nature and degree of the child's special educational needs”. Definition and Characteristics: Tourette Syndrome (TS) is a neurological disorder. It is considered to be a life-long condition that is biochemically based and genetically transmitted. Literature widely supports autosomal dominant inheritance, which means that if an individual has the disorder, there is a 50-50 chance that each offspring will inherit the gene. A neurochemical basis for TS suggests that there is an imbalance in the function of the neurotransmitter Dopamine. Estimates of prevalence can vary according to the definition employed and the design of the study. There is no cure for TS, although in many cases tics become less evident as the individual gets older. Medication such as haloperidol (Haldol), pimozide (Orap), fluphenazine (Prolixin), and clonidine (Catapres) may also help to control symptoms, which although involuntary, can be suppressed for periods of time, usually followed by an outburst of tics known as a tic storm. -
The Portrayal of Tourette Syndrome in Film and Television Samantha Calder-Sprackman, Stephanie Sutherland, Asif Doja
ORIGINAL ARTICLE COPYRIGHT ©2014 T HE CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES INC . The Portrayal of Tourette Syndrome in Film and Television Samantha Calder-Sprackman, Stephanie Sutherland, Asif Doja ABSTRACT: Objective: To determine the representation of Tourette Syndrome (TS) in fictional movies and television programs by investigating recurrent themes and depictions. Background: Television and film can be a source of information and misinformation about medical disorders. Tourette Syndrome has received attention in the popular media, but no studies have been done on the accuracy of the depiction of the disorder. Methods: International internet movie databases were searched using the terms “Tourette’s”, “Tourette’s Syndrome”, and “tics” to generate all movies, shorts, and television programs featuring a character or scene with TS or a person imitating TS. Using a grounded theory approach, we identified the types of characters, tics, and co-morbidities depicted as well as the overall representation of TS. Results: Thirty-seven television programs and films were reviewed dating from 1976 to 2010. Fictional movies and television shows gave overall misrepresentations of TS. Coprolalia was overrepresented as a tic manifestation, characters were depicted having autism spectrum disorder symptoms rather than TS, and physicians were portrayed as unsympathetic and only focusing on medical therapies. School and family relationships were frequently depicted as being negatively impacted by TS, leading to poor quality of life. Conclusions: Film and television are easily accessible resources for patients and the public that may influence their beliefs about TS. Physicians should be aware that TS is often inaccurately represented in television programs and film and acknowledge misrepresentations in order to counsel patients accordingly. -
G E O R G E S G I L L E S D E L a T O U R E T
G e o r g e s G i l l e s d e l a T o u r e t t e L i f e a n d w o r k by Hermann Krämer Translation: Dr. Christine Daniels Georges Albert Édouard Brutus Gilles de la Tourette was born on October 30th 1857 in Saint-Gervais-les-Trois-Clochers, a small village near Loudun in the département Vienne in west-central France. His father, Théodore, was a merchant and had four children, of which Gilles was the eldest. He grew up in a family that already had brought forth many physicians and scholars. Little is known about his early childhood: His education started at the boarding school of Chatellerault, where he was striking as an exceptionally talented but also restless and rebelling pupil, who often was bored by school lessons. He commenced medical studies at the University of Poitiers at the early age of 16 years and finished his studies in 1881 with great success. - 2 - Subsequently he left for Paris to continue his medical education. This time Paul le Gendre, a friend of Gilles, was describing Gilles in the following way [1]: He was a sociable man and excellent speaker with a loud, rough and slightly hoarse voice. He was very spirited, sometimes flying into a passion, and tended to become impatient. In discussions, a single contradiction made him explode and not even a great number of opponents of his representations was able to bridle and moderate him. Even in loudest and heated debates his voice could be identified easily. -
Eye Movement Measures of Cognitive Control in Children with Tourette Syndrome
The Texas Medical Center Library DigitalCommons@TMC The University of Texas MD Anderson Cancer Center UTHealth Graduate School of The University of Texas MD Anderson Cancer Biomedical Sciences Dissertations and Theses Center UTHealth Graduate School of (Open Access) Biomedical Sciences 5-2010 Eye Movement Measures of Cognitive Control in Children with Tourette Syndrome Cameron B. Jeter Follow this and additional works at: https://digitalcommons.library.tmc.edu/utgsbs_dissertations Part of the Cognitive Neuroscience Commons, Nervous System Diseases Commons, Other Psychiatry and Psychology Commons, and the Systems Neuroscience Commons Recommended Citation Jeter, Cameron B., "Eye Movement Measures of Cognitive Control in Children with Tourette Syndrome" (2010). The University of Texas MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences Dissertations and Theses (Open Access). 26. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/26 This Dissertation (PhD) is brought to you for free and open access by the The University of Texas MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences at DigitalCommons@TMC. It has been accepted for inclusion in The University of Texas MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences Dissertations and Theses (Open Access) by an authorized administrator of DigitalCommons@TMC. For more information, please contact [email protected]. EYE MOVEMENT MEASURES OF COGNITIVE CONTROL IN CHILDREN WITH TOURETTE SYNDROME by Cameron Beth -
Adulthood Outcome of Tic and Obsessive-Compulsive Symptom Severity in Children with Tourette Syndrome
ARTICLE Adulthood Outcome of Tic and Obsessive-Compulsive Symptom Severity in Children With Tourette Syndrome Michael H. Bloch, BA; Bradley S. Peterson, MD; Lawrence Scahill, MSN, PhD; Jessica Otka, BA; Lily Katsovich, MS; Heping Zhang, PhD; James F. Leckman, MD Background: Tourette syndrome (TS) is a childhood- Main Outcome Measures: Expert-rated tic and OCD onset neuropsychiatric disorder that is characterized by symptom severity at follow-up interview an average of both motor and phonic tics. One half to two thirds of chil- 7.6 years later (range, 3.8-12.8 years). dren with TS experience a reduction or complete reso- lution of tic symptoms during adolescence. At least one Results: Eighty-five percent of subjects reported a re- third of adults with TS have comorbid obsessive- duction in tic symptoms during adolescence. Only in- compulsive disorder (OCD). creased tic severity in childhood was associated with increased tic severity at follow-up. The average age at worst- Objectives: To clarify the clinical course of tic and OCD ever tic severity was 10.6 years. Forty-one percent of pa- symptoms in children with TS and determine if baseline tients with TS reported at one time experiencing at least clinical measurements in childhood are associated with moderate OCD symptoms. Worst-ever OCD symptoms future symptom severity in late adolescence and early occurred approximately 2 years later than worst-ever tic adulthood. symptoms. Increased childhood IQ was strongly associ- ated with increased OCD severity at follow-up. Design: Prospective cohort study. Conclusion: Obsessive-compulsive disorder symp- Setting: Yale Child Study Center tic and OCD outpa- tient specialty clinic.