Tic Disorders and Tourette's Syndrome are neurodevelopmental disorders, characterised by involuntary movements and vocalisations known as tics.
TS is a genetically determined neurological condition, characterised by involuntary movements and vocalisations known as tics1. TS was once regarded as a rare syndrome associated with coprolalia (the utterance of obscene words or socially inappropriate and derogatory remarks). It is now understood that TS is not rare, affecting maybe 10% of the population, but that only a small minority of those with TS have coprolalia2.
The commonest symptoms of TS are tics; sudden, rapid, repetitive movements or sounds that occur intermittently. Motor tics involve involuntary movements of specific muscle groups, such as blinking, head jerking, or shoulder shrugging. Vocal tics encompass involuntary sounds or utterances, such as throat clearing, grunting, or repeating words or phrases2.
Tics in TS typically start during childhood; peak onset is between 5 and 10 years old. TS may first present with simple motor tics, such as eye blinking or facial grimacing, followed by the emergence of more complex tics, including vocalisations or gestures. The severity and frequency of tics can fluctuate over time, with periods of exacerbation (known as tic flares) and remission3.
TS can present differently in adults. Tics may become less frequent or change in character over time; a tic can rarely present as a tremor. Adults with TS may experience a broader range of symptoms, including motor and vocal tics, as well as associated features such as obsessive-compulsive symptoms, depression anxiety, autistic spectrum disorder and attention difficulties. They may also face challenges in social and occupational functioning1,4.
While there is no cure for TS, interventions (pharmacological and non-pharmacological) can help to manage symptoms and improve quality of life. They should be tailored to specific needs and may include the following7,8,9:
Providing patients and their families with information, coping strategies, and support groups can help to enhance understanding and resilience. Encouraging a supportive and inclusive environment at home, school, and work can also contribute to improved outcomes and quality of life for individuals with TS.