NON RARE IN EUROPE: Tourette syndrome

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1FDA treatments8Treatment centers

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Overview

Tourette syndrome (TS), also known as Gilles de la Tourette syndrome or Tourette disorder, is a neurodevelopmental condition characterized by multiple motor tics and at least one vocal (phonic) tic that persist for more than one year. Tics are sudden, rapid, recurrent, nonrhythmic movements or vocalizations that typically begin in childhood, most commonly between ages 4 and 6. Motor tics often start in the face and head region (such as eye blinking, facial grimacing, or head jerking) and may progress to involve other body parts. Vocal tics can range from simple sounds like throat clearing, sniffing, or grunting to more complex vocalizations. Coprolalia (involuntary utterance of obscene words), though widely associated with the condition in popular culture, occurs in only a minority of patients (approximately 10-15%). Tourette syndrome primarily affects the nervous system, specifically involving dysfunction in cortico-striato-thalamo-cortical circuits of the brain. The condition frequently co-occurs with other neurobehavioral disorders, most notably attention deficit hyperactivity disorder (ADHD) and obsessive-compulsive disorder (OCD), which may cause more functional impairment than the tics themselves. Other common comorbidities include anxiety disorders, learning difficulties, and behavioral problems. Tic severity typically peaks during early adolescence and often improves significantly by late adolescence or early adulthood, though some individuals continue to experience tics throughout their lives. Treatment is individualized and is generally recommended when tics cause significant distress or functional impairment. Behavioral therapies, particularly Comprehensive Behavioral Intervention for Tics (CBIT) and habit reversal training, are considered first-line treatments. Pharmacological options include alpha-2 adrenergic agonists (clonidine, guanfacine), antipsychotic medications (such as aripiprazole, risperidone, and haloperidol), and medications targeting comorbid conditions. Deep brain stimulation (DBS) is being investigated for severe, treatment-refractory cases. There is currently no cure for Tourette syndrome, but many patients experience substantial improvement with appropriate management.

Also known as:

Inheritance

Multifactorial

Caused by a mix of several genes and environmental factors

Age of Onset

Childhood

Begins in childhood, roughly ages 1 to 12

Orphanet ↗NORD ↗

FDA & Trial Timeline

10 events
Feb 2026

ARIPIPRAZOLE: FDA approved

FDAcompleted
Jan 2026ABILIFY MAINTENA: New indication approved
FDAcompleted
Mar 2025ABILIFY MAINTENA: New indication approved
FDAcompleted
Mar 2025ABILIFY MAINTENA: New indication approved
FDAcompleted
Jan 2025ABILIFY MAINTENA: New indication approved
FDAcompleted
Feb 2020ABILIFY MAINTENA: New indication approved
FDAcompleted
Jul 2017ABILIFY MAINTENA: New indication approved
FDAcompleted
Feb 2017ABILIFY MAINTENA: New indication approved
FDAcompleted
Aug 2016ABILIFY MAINTENA: New indication approved
FDAcompleted
Mar 2016

ABILIFY MAINTENA: New indication approved

FDAcompleted

Data sourced from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.

Treatments

1 available

Abilify

aripiprazole· Otsuka Pharmaceutical Development■ Boxed WarningOrphan Drug

Treatment of pediatric patients with Tourette's

No actively recruiting trials found for NON RARE IN EUROPE: Tourette syndrome at this time.

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No specialists are currently listed for NON RARE IN EUROPE: Tourette syndrome.

View NORD Rare Disease Centers ↗Undiagnosed Disease Network ↗

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to NON RARE IN EUROPE: Tourette syndrome.

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Caregiver Resources

NORD Caregiver Resources

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Mental Health Support

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Financial assistance programs specifically for caregivers of rare disease patients.

Social Security Disability

Learn how rare disease patients may qualify for SSDI/SSI benefits.

Common questions about NON RARE IN EUROPE: Tourette syndrome

What is NON RARE IN EUROPE: Tourette syndrome?

Tourette syndrome (TS), also known as Gilles de la Tourette syndrome or Tourette disorder, is a neurodevelopmental condition characterized by multiple motor tics and at least one vocal (phonic) tic that persist for more than one year. Tics are sudden, rapid, recurrent, nonrhythmic movements or vocalizations that typically begin in childhood, most commonly between ages 4 and 6. Motor tics often start in the face and head region (such as eye blinking, facial grimacing, or head jerking) and may progress to involve other body parts. Vocal tics can range from simple sounds like throat clearing, sni

How is NON RARE IN EUROPE: Tourette syndrome inherited?

NON RARE IN EUROPE: Tourette syndrome follows a multifactorial inheritance pattern. Genetic counseling can help families understand recurrence risk and testing options.

At what age does NON RARE IN EUROPE: Tourette syndrome typically begin?

Typical onset of NON RARE IN EUROPE: Tourette syndrome is childhood. Age of onset can vary across affected individuals.