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Tourette syndrome and other tic disorders
1Departments of Neurology and Pediatrics, Johns Hopkins University School of Medicine, Baltimore 21287, USA. hsinger@jhmi.edu
Handbook of Clinical Neurology
|April 19, 2011
Summary
Tic disorders, like Tourette syndrome, are childhood-onset movement abnormalities with fluctuating courses. Research explores their genetic, autoimmune, and neurobiological underpinnings, impacting treatment strategies.
Area of Science:
- Neuroscience
- Genetics
- Pediatrics
Background:
- Tic disorders, including Tourette syndrome, are paroxysmal movement abnormalities originating in childhood.
- These conditions present a fluctuating clinical course and can lead to significant psychosocial and physical challenges.
- Comorbid conditions frequently accompany tic disorders, often exacerbating their overall impact.
Observation:
- Tic disorders typically improve by early adulthood.
- Current therapeutic approaches are symptomatic, encompassing educational, behavioral, and pharmacological interventions.
- The precise genetic cause remains unidentified despite evidence for an inherited basis.
Findings:
- The pathophysiology suggests alterations within cortico-striatal-thalamo-cortical circuits, though the exact location is undetermined.
- Evidence points towards abnormalities in synaptic neurotransmission, particularly involving the dopaminergic system.
- A proposed poststreptococcal autoimmune etiology for tic disorders remains a subject of controversy.
Implications:
- Understanding the neurobiological basis of tic disorders is crucial for developing targeted therapies.
- Further research into the genetic and autoimmune factors may elucidate disease mechanisms.
- Improved management strategies are needed to address the complex nature of tic disorders and their comorbidities.
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