TY - JOUR
T1 - Networks in the Field of Tourette Syndrome
AU - Kleimaker, Alexander
AU - Kleimaker, Maximilian
AU - Behm, Amelie
AU - Weissbach, Anne
AU - Bäumer, Tobias
AU - Beste, Christian
AU - Roessner, Veit
AU - Münchau, Alexander
N1 - Publisher Copyright:
© Copyright © 2021 Kleimaker, Kleimaker, Behm, Weissbach, Bäumer, Beste, Roessner and Münchau.
PY - 2021/4/13
Y1 - 2021/4/13
N2 - Gilles de la Tourette syndrome (TS) is a neuropsychiatric neurodevelopmental disorder with the cardinal clinical features of motor and phonic tics. Clinical phenomenology can be complex since, besides tics, there are other features including premonitory urges preceding tics, pali-, echo-, and coprophenomena, hypersensitivity to external stimuli, and symptom dependency on stress, attention, and other less well-defined factors. Also, the rate of comorbidities, particularly attention deficit hyperactivity disorder and obsessive-compulsive disorder, is high. Mirroring the complexities of the clinical course and phenomenology, pathophysiological findings are very diverse, and etiology is disputed. It has become clear, though, that abnormalities in the basal ganglia and their connections with cortical areas are key for the understanding of the pathophysiology and as regards etiology, genetic factors are crucial. Against this background, both adequate clinical management of TS and TS-related research require multidisciplinary preferably international cooperation in larger groups or networks to address the multiple facets of this disorder and yield valid and useful data. In particular, large numbers of patients are needed for brain imaging and genetic studies. To meet these requirements, a number of networks and groups in the field of TS have developed over the years creating an efficient, lively, and supportive international research community. In this review, we will provide an overview of these groups and networks.
AB - Gilles de la Tourette syndrome (TS) is a neuropsychiatric neurodevelopmental disorder with the cardinal clinical features of motor and phonic tics. Clinical phenomenology can be complex since, besides tics, there are other features including premonitory urges preceding tics, pali-, echo-, and coprophenomena, hypersensitivity to external stimuli, and symptom dependency on stress, attention, and other less well-defined factors. Also, the rate of comorbidities, particularly attention deficit hyperactivity disorder and obsessive-compulsive disorder, is high. Mirroring the complexities of the clinical course and phenomenology, pathophysiological findings are very diverse, and etiology is disputed. It has become clear, though, that abnormalities in the basal ganglia and their connections with cortical areas are key for the understanding of the pathophysiology and as regards etiology, genetic factors are crucial. Against this background, both adequate clinical management of TS and TS-related research require multidisciplinary preferably international cooperation in larger groups or networks to address the multiple facets of this disorder and yield valid and useful data. In particular, large numbers of patients are needed for brain imaging and genetic studies. To meet these requirements, a number of networks and groups in the field of TS have developed over the years creating an efficient, lively, and supportive international research community. In this review, we will provide an overview of these groups and networks.
UR - http://www.scopus.com/inward/record.url?scp=85104965975&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/a95da33b-5460-3456-b1a3-309000921984/
U2 - 10.3389/fneur.2021.624858
DO - 10.3389/fneur.2021.624858
M3 - Scientific review articles
C2 - 33927678
AN - SCOPUS:85104965975
SN - 1664-2295
VL - 12
SP - 624858
JO - Frontiers in Neurology
JF - Frontiers in Neurology
M1 - 624858
ER -