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Tourette's Syndrome

Tourette's Syndrome is a neurodevelopmental disorder characterized by multiple motor and one or more vocal tics persisting for more than one year. Onset occurs before age 18, typically between ages 4-6 years, with a prevalence of 0.3-1% in school-age children.

Key Points

  • Childhood-onset neurological disorder
  • Multiple motor and vocal tics are hallmark features
  • Strong genetic component with complex inheritance
  • High rate of neurobehavioral comorbidities
  • Waxing and waning course is typical

Motor Tics

Simple Motor Tics

  • Eye blinking
  • Facial grimacing
  • Head jerking
  • Shoulder shrugging
  • Nose twitching

Complex Motor Tics

  • Touching objects or others
  • Hopping or jumping
  • Copropraxia (obscene gestures)
  • Echopraxia (mimicking others' movements)
  • Self-injurious behaviors

Vocal Tics

Simple Vocal Tics

  • Throat clearing
  • Sniffing
  • Grunting
  • Coughing
  • Whistling

Complex Vocal Tics

  • Coprolalia (obscene words)
  • Echolalia (repeating others' words)
  • Palilalia (repeating own words)
  • Words or phrases out of context

Diagnostic Criteria (DSM-5)

  • Multiple motor tics
  • One or more vocal tics
  • Tics present for >1 year
  • Onset before age 18
  • Not due to substance use or medical condition

Clinical Assessment

  • Detailed history including:
    • Age of onset
    • Tic progression
    • Family history
    • Impact on daily functioning
  • Physical and neurological examination
  • Yale Global Tic Severity Scale (YGTSS)
  • Premonitory Urge for Tics Scale (PUTS)

Differential Diagnosis

  • Transient tic disorder
  • Chronic motor or vocal tic disorder
  • OCD
  • ADHD
  • Stereotypic movement disorder
  • Myoclonus

Treatment Approach

Behavioral Interventions

  • Comprehensive Behavioral Intervention for Tics (CBIT)
  • Habit Reversal Training (HRT)
  • Exposure and Response Prevention (ERP)
  • Relaxation techniques
  • Parent training and education

Pharmacological Treatment

First-line Medications

  • Alpha-2 agonists
    • Clonidine (0.05-0.3 mg/day)
    • Guanfacine (0.5-4 mg/day)

Second-line Medications

  • Antipsychotics
    • Risperidone (0.5-3 mg/day)
    • Aripiprazole (2.5-20 mg/day)
    • Haloperidol (0.25-3 mg/day)
  • Topiramate
  • Baclofen

Emerging Therapies

  • Deep Brain Stimulation (severe cases)
  • Cannabinoids (under investigation)
  • Novel pharmacological agents

Common Comorbid Conditions

Neurobehavioral

  • ADHD (50-60%)
  • OCD (30-50%)
  • Anxiety disorders (40%)
  • Depression (30%)
  • Learning disabilities (20%)
  • Executive function deficits

Other Associated Conditions

  • Sleep disorders
  • Migraine headaches
  • Rage attacks
  • Social skills deficits
  • Sensory processing issues

Impact on Quality of Life

  • Academic difficulties
  • Social challenges
  • Family stress
  • Occupational impairment
  • Emotional regulation difficulties

Natural History

  • Peak severity: 10-12 years
  • Improvement in adolescence: 60-80%
  • Adult persistence: 20-30%

Prognostic Factors

Poor Prognostic Indicators

  • Early onset
  • Multiple comorbidities
  • Family history
  • Severe initial symptoms

Good Prognostic Indicators

  • Later onset
  • Minimal comorbidities
  • Good social support
  • Early intervention

Long-term Monitoring

  • Regular assessment of tic severity
  • Monitoring for comorbidities
  • Academic/occupational support
  • Family support and counseling
  • Transition planning for adolescents
Further Reading


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