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In This Topic
Pediatrics
Neurologic Disorders in Children
Tourette's Syndrome
Symptoms and Signs
Diagnosis
Treatment
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Chapters in Pediatrics
  • Introduction
  • Approach to the Care of Normal Infants and Children
  • Approach to the Care of Adolescents
  • Caring for Sick Children and Their Families
  • Growth and Development
  • Principles of Drug Treatment in Children
  • Perinatal Physiology
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  • Mental Disorders in Children and Adolescents
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  • Incontinence in Children
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  • Human Immunodeficiency Virus (HIV) Infection in Infants and Children
Topics in Neurologic Disorders in Children
  • Cerebral Palsy (CP) Syndromes
  • Febrile Seizures
  • Infantile Spasms
  • Neonatal Seizure Disorders
  • Tourette's Syndrome
     
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    Tourette's Syndrome(Gilles de la Tourette's Syndrome)

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    Tourette's syndrome is a hereditary tic disorder that begins during childhood. Symptoms include simple, complex, and vocal tics. Diagnosis is clinical. Treatment may include clonidine and antipsychotics.

    Tourette's syndrome is probably autosomal dominant with variable penetrance; the specific genetic abnormality is unknown. Male:female ratio is 3:1. Simple transient tics, chronic tic disorder, and Tourette's syndrome form a continuum or spectrum.

    Symptoms and Signs

    The movement disorder may begin with simple tics (eg, facial grimacing, head jerking, blinking, sniffing) that progress to multiple complex tics, including respiratory and vocal ones (eg, loud, irritating vocalizations; snorting). Vocal tics may begin as grunting or barking noises and evolve into compulsive utterances that are often loud or shrill. Patients may voluntarily suppress tics for seconds or minutes. Coprolalia (involuntary scatologic or obscene utterances) occurs in a few patients. Severe tics and coprolalia are physically and socially disabling. Echolalia (immediate repetition of one's own or another person's words or phrases) is common. In most children, tics tend to wane during the teenage years.

    Comorbid disorders (eg, attention-deficit/hyperactivity disorder, obsessive-compulsive disorder, learning disabilities, anxiety) and poor socialization are common and may be more problematic and more likely to need intervention than the tics.

    Diagnosis

    • Clinical evaluation

    Diagnosis is clinical. To differentiate Tourette's syndrome from transient tics, physicians may have to monitor patients over time.

    Treatment

    • ClonidineSome Trade Names
      CATAPRES
      Click for Drug Monograph
    • Sometimes antipsychotics

    Treatment to suppress tics is recommended only if they are significantly interfering with the children's activities or self-image; treatment does not alter the natural history of the disorder. ClonidineSome Trade Names
    CATAPRES
    Click for Drug Monograph
    0.05 to 0.1 mg po tid or qid is effective in some patients. Adverse effects of fatigue may limit dosage; hypotension is uncommon.

    Antipsychotics (eg, risperidoneSome Trade Names
    RISPERDAL
    Click for Drug Monograph
    0.25 to 1.5 mg po bid, haloperidolSome Trade Names
    HALDOL
    Click for Drug Monograph
    0.5 to 2 mg po bid or tid, pimozideSome Trade Names
    ORAP
    Click for Drug Monograph
    1 to 2 mg po bid, olanzapineSome Trade Names
    ZYPREXA
    Click for Drug Monograph
    2.5 to 5 mg once/day) may be required. The lowest dose required to make tics tolerable is used; doses are tapered as tics wane. Adverse effects of dysphoria, parkinsonism, akathisia, and tardive dyskinesia may limit use of antipsychotics; using lower daytime doses and higher bedtime doses may decrease adverse effects.

    Last full review/revision May 2009 by Margaret C. McBride, MD

    Content last modified February 2012

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