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Journal articles on the topic 'Tourette’s Syndrome'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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1

Dhamayanti, Meita, Isabella Riandani, and Lelly Resna. "Tourette’s syndrome." Paediatrica Indonesiana 44, no. 1 (October 10, 2016): 37. http://dx.doi.org/10.14238/pi44.1.2004.37-40.

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The aim of this report was to show that mostbehavioral disorders need multidisciplinary manage-ment by behaviorist, neurologist, psychiatrist, psy-chologist and pedagogue, and to give more informa-tion about Tourette’s syndrome so that it can be de-tected earlier. Therefore, children who suffer from itcan live a better life and develop their ability.

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2

Gilbert, Donald L., and Tara D. Lipps. "Tourette’s syndrome." Current Treatment Options in Neurology 7, no. 3 (June 2005): 211–19. http://dx.doi.org/10.1007/s11940-005-0014-2.

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3

Svyrydova, N. K., Y. O. Trufanov, A. V. Artemenko, A. M. Rakhnianska, and S. O. Schurevskyy. "The Tourette’s syndrome: clinical case." East European Journal of Neurology, no. 1(7) (March 20, 2016): 12–17. http://dx.doi.org/10.33444/2411-5797.2016.1(7).12-17.

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Tourette’s Syndrome (TS) — is the complex of symptoms of affection of the central nervous system, characterized by paroxysmal (rarely permanent) tic muscle twitching of face, neck, upper and lower extremities, hyperkinesia of respiratory muscles and facial muscles with involuntary exclamations of impulsive individual sounds or words [1]. The disease has an autosomal recessive inheritance and with disease onset in children aged 2 to 14 years, and boys get sick 2-3 times more likely than girls. Pathology does not affect life expectancy and mental development [2]. This article describes a case of clinical practice follow up female patient with Tourette's syndrome. The attention is focused on the methods of examination and differential diagnosis of this disease. TS’s studies has a perspective in creation of evidence base, early detection and treatment, also in prevention of underdiagnosis of this pathology.

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4

Stern, Jeremy S. "Tourette’s syndrome and its borderland." Practical Neurology 18, no. 4 (April 10, 2018): 262–70. http://dx.doi.org/10.1136/practneurol-2017-001755.

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The Gilles de la Tourette syndrome (or Tourette’s syndrome) has a prevalence of 1% of children with a wide range of severity and associated comorbidities. The last 20 years have seen advances in the understanding of the syndrome’s complex genetics and underlying neurobiology. Investigation with imaging and neurophysiology techniques indicate it is a neurodevelopmental condition with dysfunction of basal ganglia–cortical interactions, which are now also being studied in animal models. There is also increasing evidence for treatments although it often remains difficult to manage. First-line options include neuroleptics, other drugs and specialised behavioural treatments. Deep brain stimulation is an evolving field, not yet fully established. This review focuses on the phenomenology of tics, how to assess and manage the syndrome, and uses examples of atypical cases to explore the characteristics and limits of its clinical spectrum.

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5

Millichap, J. Gordon. "Prognosis of Tourette’s Syndrome." Pediatric Neurology Briefs 6, no. 5 (May 1, 1992): 37. http://dx.doi.org/10.15844/pedneurbriefs-6-5-7.

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6

Rindner, Ellen C. "Living with Tourette’s Syndrome." Journal of Psychosocial Nursing and Mental Health Services 45, no. 8 (August 1, 2007): 19–23. http://dx.doi.org/10.3928/02793695-20070801-05.

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7

Mittal, Shivam Om. "Tics and Tourette’s syndrome." Drugs in Context 9 (March 30, 2020): 1–7. http://dx.doi.org/10.7573/dic.2019-12-2.

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8

Wodrich, David L. "Tourette’s Syndrome and Tics." Journal of School Psychology 36, no. 3 (September 1998): 281–94. http://dx.doi.org/10.1016/s0022-4405(98)00011-9.

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9

Donaher, Joseph. "Tourette’s Syndrome and Stuttering." Perspectives on Fluency and Fluency Disorders 16, no. 2 (September 2006): 5–6. http://dx.doi.org/10.1044/ffd16.2.5.

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10

Swain, James E., and James F. Leckman. "Tourette’s syndrome in children." Current Treatment Options in Neurology 5, no. 4 (July 2003): 299–308. http://dx.doi.org/10.1007/s11940-003-0036-6.

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11

Teive, Hélio A. G., Adriana Moro, Mariana Moscovich, and Renato P. Munhoz. "Increased sexual arousal in patients with movement disorders." Arquivos de Neuro-Psiquiatria 74, no. 4 (April 2016): 303–6. http://dx.doi.org/10.1590/0004-282x20150217.

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ABSTRACT Increased of sexual arousal (ISA) has been described in different neurological diseases. The purpose of this study was present a case series of ISA in patients with movement disorders. Method Fifteen patients with different forms of movement disorders (Parkinson’s disease, Huntington’s disease, Tourette´s syndrome, spinocerebellar ataxia type 3), were evaluated in the Movement Disorders Unit of the Federal University of Paraná. Results Among Parkinson’s disease patients there were seven cases with different forms of ISA due to dopaminergic agonist use, levodopa abuse, and deep brain stimulation (DBS). In the group with hyperkinetic disorders, two patients with Huntington’s disease, two with Tourette’s syndrome, and four with spinocerebellar ataxia type 3 presented with ISA. Conclusions ISA in this group of patients had different etiologies, predominantly related to dopaminergic treatment or DBS in Parkinson’s disease, part of the background clinical picture in Huntington’s disease and Tourette’s syndrome, and probably associated with cultural aspects in patients with spinocerebellar ataxia type 3.

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12

Calder-Sprackman, Samantha, Stephanie Sutherland, and Asif Doja. "The Portrayal of Tourette Syndrome in Film and Television." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 41, no. 2 (March 2014): 226–32. http://dx.doi.org/10.1017/s0317167100016620.

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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.

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13

Millichap, J. Gordon. "Tic Disorders and Tourette’s Syndrome." Pediatric Neurology Briefs 9, no. 9 (September 1, 1995): 66. http://dx.doi.org/10.15844/pedneurbriefs-9-9-2.

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14

Millichap, J. Gordon. "Eary Signs of Tourette’s Syndrome." Pediatric Neurology Briefs 7, no. 10 (October 1, 1993): 80. http://dx.doi.org/10.15844/pedneurbriefs-7-10-12.

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15

Millichap, J. Gordon. "Learning Disabilities and Tourette’s Syndrome." Pediatric Neurology Briefs 10, no. 9 (September 1, 1996): 69. http://dx.doi.org/10.15844/pedneurbriefs-10-9-7.

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16

Millichap, J. Gordon. "Metabolic Anatomy of Tourette’s Syndrome." Pediatric Neurology Briefs 11, no. 5 (May 1, 1997): 38. http://dx.doi.org/10.15844/pedneurbriefs-11-5-11.

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17

Millichap, J. Gordon. "Tourette’s Syndrome and Neurofibromatosis 1." Pediatric Neurology Briefs 14, no. 9 (September 1, 2000): 69. http://dx.doi.org/10.15844/pedneurbriefs-14-9-9.

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18

Coffey, Barbara J. "Anxiety Disorders in Tourette’s Syndrome." Child and Adolescent Psychiatric Clinics of North America 2, no. 4 (October 1993): 709–25. http://dx.doi.org/10.1016/s1056-4993(18)30535-2.

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19

Camargo, C., A. Bronzini, C. Medyk, F. Berbetz, J. Sabattini, and M. Young-Blood. "Tourette’s syndrome in famous musicians." Journal of the Neurological Sciences 357 (October 2015): e238. http://dx.doi.org/10.1016/j.jns.2015.08.834.

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20

Jankovic, Joseph, Carolyn Kwak, and Richard Frankoff. "Tourette’s Syndrome and the Law." Journal of Neuropsychiatry and Clinical Neurosciences 18, no. 1 (February 2006): 86–95. http://dx.doi.org/10.1176/jnp.18.1.86.

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21

Poulter, Caroline, and Jonathan Mills. "Tourette’s syndrome and tic disorders." InnovAiT: Education and inspiration for general practice 11, no. 7 (May 25, 2018): 362–65. http://dx.doi.org/10.1177/1755738017740914.

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Tourette’s syndrome and tic disorders affect around 1% of the population. The presentation can range from relatively innocuous stereotyped movements and noises, through to more severe symptoms resulting in significant social and psychological disability. Although the majority of tic disorders present in childhood, a third of those affected experience tics into adulthood. The prevalence suggests that most GPs will have patients with tic disorders in their practice.

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22

STEWART, JONATHAN T., and LEONARD S. WILLIAMS. "Tourette’s-Like Syndrome and Dementia." American Journal of Psychiatry 160, no. 7 (July 2003): 1356–57. http://dx.doi.org/10.1176/appi.ajp.160.7.1356.

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23

Duda, Laura, and Gayatra Mainali. "Pharmaceutical Interventions for Tourette’s Syndrome." Current Developmental Disorders Reports 3, no. 4 (October 29, 2016): 213–16. http://dx.doi.org/10.1007/s40474-016-0098-2.

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24

Plessen, Kerstin J. "Tic disorders and Tourette’s syndrome." European Child & Adolescent Psychiatry 22, S1 (December 7, 2012): 55–60. http://dx.doi.org/10.1007/s00787-012-0362-x.

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25

Kurlan, Roger. "Tourette’s syndrome: Are stimulants safe?" Current Neurology and Neuroscience Reports 3, no. 4 (July 2003): 285–88. http://dx.doi.org/10.1007/s11910-003-0004-2.

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26

Ludlow, Amanda K., Rachel Brown, and Joerg Schulz. "A qualitative exploration of the daily experiences and challenges faced by parents and caregivers of children with Tourette’s syndrome." Journal of Health Psychology 23, no. 14 (September 28, 2016): 1790–99. http://dx.doi.org/10.1177/1359105316669878.

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Few studies address the daily challenges faced by parents of children diagnosed with Tourette’s syndrome. This article reports on a qualitative interview study with 15 parents exploring their experiences, the challenges they face and the support mechanisms they have found to be most helpful. Thematic analysis identified four core categories which represented shared experiences of the participants: coping with children’s challenging behaviours, misconceptions and lack of understanding of professionals and the lay public, negative experiences of their children’s education and lack of support and services for families with Tourette’s syndrome. The findings highlight the challenges of parenting a child with Tourette’s syndrome, particularly with respect to family life and the child’s schooling.

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27

Zykov, V. P. "Tics and Tourette’s syndrome in children." Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova 120, no. 5 (2020): 116. http://dx.doi.org/10.17116/jnevro2020120051116.

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28

Millichap, J. Gordon. "Tourette’s Syndrome and Stimulus-Induced Tics." Pediatric Neurology Briefs 8, no. 8 (August 1, 1994): 63. http://dx.doi.org/10.15844/pedneurbriefs-8-8-10.

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29

Millichap, J. Gordon. "Treatment of ADHD in Tourette’s Syndrome." Pediatric Neurology Briefs 9, no. 1 (January 1, 1995): 6. http://dx.doi.org/10.15844/pedneurbriefs-9-1-8.

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30

Millichap, J. Gordon. "Deprenyl in Tourette’s Syndrome and ADHD." Pediatric Neurology Briefs 10, no. 5 (May 1, 1996): 40. http://dx.doi.org/10.15844/pedneurbriefs-10-5-14.

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31

Millichap, J. Gordon. "Corpus Callosum Size in Tourette’s Syndrome." Pediatric Neurology Briefs 10, no. 9 (September 1, 1996): 68. http://dx.doi.org/10.15844/pedneurbriefs-10-9-6.

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32

Ackermans, Linda, Yasin Temel, and Veerle Visser-Vandewalle. "Deep brain stimulation in Tourette’s syndrome." Neurotherapeutics 5, no. 2 (April 2008): 339–44. http://dx.doi.org/10.1016/j.nurt.2008.01.009.

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33

Peterson, Bradley S., and Joel E. Klein. "Neuroimaging of Tourette’s Syndrome Neurobiologic Substrate." Child and Adolescent Psychiatric Clinics of North America 6, no. 2 (April 1997): 343–64. http://dx.doi.org/10.1016/s1056-4993(18)30308-0.

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34

Müller-Vahl, Kirsten R. "Cannabinoids reduce symptoms of Tourette’s syndrome." Expert Opinion on Pharmacotherapy 4, no. 10 (October 2003): 1717–25. http://dx.doi.org/10.1517/14656566.4.10.1717.

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35

Cosentino, Carlos, and Luis Torres. "Tourette’s syndrome and neurofibromatosis type 1." Pediatric Neurology 22, no. 5 (May 2000): 420–21. http://dx.doi.org/10.1016/s0887-8994(00)00124-7.

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36

BORTOLATO, MARCO, ANTONELLA MURONI, and FRANCESCO MARROSU. "Treatment of Tourette’s Syndrome With Finasteride." American Journal of Psychiatry 164, no. 12 (December 2007): 1914–15. http://dx.doi.org/10.1176/appi.ajp.2007.07060978.

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37

ABUZZAHAB, F. S., and VICTORIA L. BROWN. "Control of Tourette’s Syndrome With Topiramate." American Journal of Psychiatry 158, no. 6 (June 2001): 968. http://dx.doi.org/10.1176/appi.ajp.158.6.968.

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38

Taylor, Jane R., Syed A. Morshed, Salina Parveen, Marcos T. Mercadante, Lawrence Scahill, Bradley S. Peterson, Robert A. King, James F. Leckman, and Paul J. Lombroso. "An Animal Model of Tourette’s Syndrome." American Journal of Psychiatry 159, no. 4 (April 2002): 657–60. http://dx.doi.org/10.1176/appi.ajp.159.4.657.

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39

Sun, Bomin, Scott E. Krahl, Shikun Zhan, and Jiankang Shen. "Improved Capsulotomy for Refractory Tourette’s Syndrome." Stereotactic and Functional Neurosurgery 83, no. 2-3 (2005): 55–56. http://dx.doi.org/10.1159/000086673.

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40

Khoury, Rita. "Mothers of children with Tourette’s syndrome." Interdyscyplinarne Konteksty Pedagogiki Specjalnej, no. 19 (September 9, 2018): 171–99. http://dx.doi.org/10.14746/ikps.2017.19.11.

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The purpose of this study was to gather data from the mothers of children with Tourette Syndrome (TS), in order to examine the extent to which the existence of a child with TS in the family affected mothers’ Quality of Life (QOL). The research was conducted according to the qualitative methods. Data was collected from semistructures interviews with 50 mothers of children with TS. The interviews were analyzed using a content analysis method. Conclusions derived from the research findings found that lack of accurate diagnosis and information leaded mothers to a state of imbalance and great stress. When they were given accurate information, they seemed to be more able to advocate for the child with TS and thus preventmisunderstandings, and consequent unpleasant situations and confusion.

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41

Lin, Jainn-Jim, Huei-Shyong Wang, Mun-Ching Wong, Chieh-Tsai Wu, and Kuang-Lin Lin. "Tourette’s syndrome with cervical disc herniation." Brain and Development 29, no. 2 (March 2007): 61–63. http://dx.doi.org/10.1016/j.braindev.2006.05.009.

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42

Buzan, Randall D., Jay H. Shore, Christopher O’Brien, and Christopher Schneck. "Obsessive-compulsive disorder and Tourette’s syndrome." Current Treatment Options in Neurology 2, no. 2 (March 2000): 125–39. http://dx.doi.org/10.1007/s11940-000-0014-1.

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43

Fernandez, Thomas V., Robert A. King, and Christopher Pittenger. "Tourette’s Syndrome and Translational Clinical Science." Journal of the American Academy of Child & Adolescent Psychiatry 54, no. 1 (January 2015): 6–8. http://dx.doi.org/10.1016/j.jaac.2014.11.004.

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44

Baweja, Raman, and Debra Byler. "Tourette’s Syndrome and Comorbid Neurological Condition." Current Developmental Disorders Reports 4, no. 3 (June 9, 2017): 61–63. http://dx.doi.org/10.1007/s40474-017-0113-2.

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45

Kumari, R. "Multimodal Dietary Treatment in Tourette’s Syndrome." Journal of the Academy of Nutrition and Dietetics 117, no. 9 (September 2017): A59. http://dx.doi.org/10.1016/j.jand.2017.06.179.

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46

Lewis, Kendra, Leonard Rappa, Devon A. Sherwood-Jachimowicz, and Margareth Larose-Pierre. "Aripiprazole for the Treatment of Adolescent Tourette’s Syndrome." Journal of Pharmacy Practice 23, no. 3 (March 31, 2010): 239–44. http://dx.doi.org/10.1177/0897190009358771.

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Gilles de la Tourette syndrome (GTS) is a neuropsychiatric, lifelong disorder with onset in childhood. The essential features of this disorder are multiple motor tics and one or more vocalizations. The neurochemical pathophysiology of GTS involves an unknown abnormality in the central dopaminergic system. Atypical antipsychotics, such as aripiprazole, serve as a new therapeutic option for GTS. The authors describe a unique case of Tourette’s syndrome (TS) in an adolescent in which aripiprazole resolved the patient’s symptoms. A 17-year-old, 5′11′′ tall, African American male weighing 220 lbs was diagnosed with TS at 9 years old. By age 16, the patient developed prominent symptoms of intermitted eye blinking, forehead raising, finger snapping, heavy breathing, and head bobbing. Clonidine, in addition to homeopathic remedies ( N-acetylcholine and alpha lipoic acid), was administered to the patient without significant diminution of symptoms. Later, aripiprazole was initiated at 5 mg/d. As a result, noticeable symptomatic improvement occurred within 48 hours. Aripiprazole was titrated over the next 4 weeks to 6.5 mg/d, with significant results. Over the next 6 months, aripiprazole was titrated again to 10 mg/d with additional symptom reduction. This case illustrates a patient who responded to aripiprazole with no reported adverse effects, when standard therapy failed to improve symptoms.

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47

Hussain, Humaira. "PRESENCE OF DYSPHONIA IN INDIVIDUALS WITH TOURETTE’S SYNDROME." Pakistan Journal of Rehabilitation 4, no. 1 (January 10, 2015): 42–47. http://dx.doi.org/10.36283/pjr.zu.4.1/009.

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Professionals working in the field of voice disorders have come to recognize the variability of vocal qualities in different populations. While voice disorders can be of organic, neurogenic, or functional etiology, concomitant disorders often directly impact the vocal features. Such a disorder is Tourette’s Syndrome which is an impairment characterized by motor and vocal tics. This study examined the prevalence of voice disorders in individuals with Tourette’s Syndrome. Research was conducted over the duration of two years with clientele aged 15;2 to 26;5. Participants were receiving continuous treatment from a team of neurologist and psychologist at private clinics situated around a suburban area. Two case studies consisting of 1-2 individuals were also closely examined to further distinguish the types of voice disorders present given the severity of motor and vocal tics. Instrumental and perceptual analysis was obtained to accurately diagnose the voice disorder. Given the sample of participants, presence of spasmodic dysphonia and falsetto were noted. Results of this study indicates a strong presence of dysphonia in individuals with Tourette’s Syndrome, particularly spasmodic dysphonia and falsetto. Additionally, dysphonic vocal qualities were irrelevant to the existence of vocal tics. Further research with this population is mandated to determine assessment and treatment strategies

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48

Millichap, J. Gordon. "Guanfacine in Comorbid ADHD & Tourette’s Syndrome." Pediatric Neurology Briefs 9, no. 9 (September 1, 1995): 66. http://dx.doi.org/10.15844/pedneurbriefs-9-9-3.

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49

Millichap, J. Gordon. "Basal Ganglia and MRI in Tourette’s Syndrome." Pediatric Neurology Briefs 7, no. 6 (June 1, 1993): 43. http://dx.doi.org/10.15844/pedneurbriefs-7-6-4.

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50

Millichap, J. Gordon. "Learning Disabilities in Tourette’s Syndrome & ADHD." Pediatric Neurology Briefs 10, no. 5 (May 1, 1996): 40. http://dx.doi.org/10.15844/pedneurbriefs-10-5-13.

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