Clinical features of Tourette syndrome and tic disorders
نویسندگان
چکیده
منابع مشابه
Tic & Tourette Syndrome and Motor Disorders
Motor disorder refers to neuropsychiatric disorders such as abnormal movements, meaningless repetitive movements, and impairment in acquisition and performance of motor skills. Motor disorder was included as a sub-category of neurodevelopmental disorder chapter in the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) [1]. DSM-5’s motor disorders include tic disorders (T...
متن کاملTourette syndrome and tic disorders: a decade of progress.
OBJECTIVE This is a review of progress made in the understanding of Tourette syndrome (TS) during the past decade including models of pathogenesis, state-of-the-art assessment techniques, and treatment. METHOD Computerized literature searches were conducted under the key words "Tourette syndrome," "Tourette disorder," and "tics." Only references from 1996-2006 were included. RESULTS Studies...
متن کاملTourette syndrome: not just a tic disorder.
Although tics are considered the hallmark of Tourette syndrome, arguably tics may not be the only or primary presenting symptom. For many children diagnosed with Tourette syndrome irritability, frustration intolerance, hyperactivity, inattention, ritual behavior or other difficulties may have been present a number of years before the appearance of tics. Children with Tourette syndrome are often...
متن کاملFamilial Risks of Tourette Syndrome and Chronic Tic Disorders. A Population-Based Cohort Study.
IMPORTANCE Tic disorders, including Tourette syndrome (TS) and chronic tic disorders (CTDs), are assumed to be strongly familial and heritable. Although gene-searching efforts are well under way, precise estimates of familial risk and heritability are lacking. Previous controlled family studies were small and typically conducted within specialist clinics, resulting in potential ascertainment bi...
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ژورنال
عنوان ژورنال: Journal of Obsessive-Compulsive and Related Disorders
سال: 2014
ISSN: 2211-3649
DOI: 10.1016/j.jocrd.2014.03.004