Tic Disorders: by Rawan Chakas

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Tic Disorders

BY RAWAN CHAKAS
Outline Epidemiology

Definition & Diagnostic criteria

Etiology

Treatment

Course & Prognosis

Tourette’s disorder, Persistent motor or vocal


tic disorder and Provisional tic disorder
What are tics?

 Tics are sudden, rapid, repetitive, stereotyped movements or vocalizations


 Tics may be simple or complex
 Although experienced as involuntary, patients can learn to temporarily
suppress tics.
 Prior to the tic, patients may feel a premonitory urge (somatic sensation), with
subsequent tension release after the tic.
 Anxiety, excitement, and fatigue can be aggravating factors for tics.
Epidemiology
 Transient tic behaviors: common in children.

 Tourette’s disorder: 3 / 1000 school-age child.

 Prevalence: boys > girls.


Motor Tics
Vocal tics

 Barking

 Coprolalia - utterance of obscene, taboo words as


an abrupt, sharp bark or grunt.

 Echolalia - repeating others’ words.


Tourette’s Disorder
 Multiple motor and at least 1 vocal tics (not
DSM-V required to occur concurrently)

Criteria  Symptoms should be present for more than 1 year


since onset of first tic.
 Onset prior to age 18 years.
 Not caused by a substance (e.g., cocaine) or another
medical condition (e.g. Huntington disease).

 One of the few psychiatric disorders in which


diagnostic criteria do not require symptoms to cause
significant distress
 Tourette’s disorder is the most severe of the tic disorders

 Vocal tics may appear many years after the motor tics, and they may wax and
wane in frequency.

 The most common motor tics involve the face and head, such as eye blinking
and throat clearing.
Etiology

 Genetic factors: >55% concordance rate in monozygotic twins.

 Prenatal/perinatal factors: Older paternal age, obstetrical complications, maternal


smoking, and low birth weight.

 Psychological factors: Symptom exacerbations with stressful life events.


Etiology

 TS seems to be an inherited developmental disorder of synaptic


neurotransmission. Further studies are needed to elucidate the physiologic and
cellular mechanisms underlying tics and TS.

 The basal ganglia, particularly the caudate nucleus and the inferior prefrontal
cortex, are implicated in the pathogenesis of TS.

 Volumetric magnetic resonance imaging studies have shown that children with
TS have larger dorsolateral prefrontal regions as well as increased cortical
white matter in the right frontal lobe.
Treatment

 Psychoeducation.
 Behavioral interventions - habit reversal therapy.
 Medications - use only if tics become severely impairing or also treating
comorbidities. Due to the fluctuating course of the disorder, it can be difficult to
determine medication efficacy.
 Alpha-2 agonists: guanfacine (first choice), clonidine (more sedating).
 In severe cases, can consider treatment with atypical (e.g. risperidone) or
typical antipsychotics (e.g. pimozide).
Course & Prognosis

 Onset typically occurs between 4 and 6 years, with the peak severity between ages
10 and 12.
 Tics wax and wane and change in type.
 Symptoms tend to decrease in adolescence and significantly diminish in
adulthood.
 Two thirds of children with TS can expect a significant amelioration of or
almost complete remission. Lifelong remissions are rare, however.
 High comorbidity with OCD, ADHD, learning disability, and autism spectrum
disorder.
References

 DSM-V
 MedScape - https://emedicine.medscape.com/article/289457-overview
Thank you

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