Tourette Syndrome Child
TS may be a genetic condition, passed from parents to children. This is still being studied. TS may also be linked to problems with dopamine levels, a chemical in the brain that sends signals to neurons.
|TS may be inherited through genes, which make up DNA.|
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Symptoms can range from mild to severe. They can occur suddenly, and the length of time they last can vary. Tics may temporarily decrease with concentration or distraction. During times of stress, they may occur more often.
Tics can be muscle movements (motor tics) or vocal sounds (vocal tics). They can also be characterized as simple or complex. Here are some common examples:
- Simple—eye blinking, facial grimacing, head jerking, arm or leg thrusting
- Complex—jumping, smelling, touching things or other people, twirling around
- Simple—throat clearing, coughing, sniffing, grunting, yelping, barking
- Complex—saying words or phrases that do not make sense in a given situation, saying obscene or socially unacceptable words (called coprolalia)
Your child may also have other related conditions, such as:
- Attention deficit disorder with or without hyperactivity (ADD or ADHD)
- Obsessive compulsive disorder (OCD)
Work with the doctor to create a treatment plan that is right for your child. Options include:
Education and Counseling
One important part of treatment is for the child and his family to learn about this syndrome. It is also helpful if the child’s teachers, classmates, and friends understand the condition.
Your child may also benefit from behavior therapy. This can include doing relaxation techniques and self-monitoring. A technique known as “habit reversal therapy” and other behavioral treatments have proven helpful for some children.
In most cases, medication is not needed to treat TS. If tics are severe and disrupt your child’s life, medications may be advised to reduce symptoms. If medication is ineffective or otherwise not right for your child, several experimental non-drug treatments have shown promise. Among these are magnetic brain stimulation and—for severely affected children—deep brain stimulation.
This content is reviewed regularly and is updated when new and relevant evidence is made available. This information is neither intended nor implied to be a substitute for professional medical advice. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with questions regarding a medical condition.
Edits to original content made by Denver Health.
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National Institute of Neurological Disorders and Stroke http://www.ninds.nih.gov
Tourette Syndrome Association, Inc. http://www.tsa-usa.org
Tourette Syndrome Association of Ontario http://www.tourettesyndromeontario.ca
Tourette Syndrome Foundation of Canada http://www.tourette.ca
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