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The association of primary dystonia with tics – chance or new syndrome?

C. Del Gamba, A. Latorre, U. Bonuccelli, R. Ceravolo, K. Bhatia (London, United Kingdom)

Meeting: 2018 International Congress

Abstract Number: 727

Keywords: Dystonia: Clinical features, Tics(also see Gilles de la Tourette syndrome): Clinical features

Session Information

Date: Sunday, October 7, 2018

Session Title: Dystonia

Session Time: 1:45pm-3:15pm

Location: Hall 3FG

Objective: This study aimed to evaluate the association between dystonia and tics as a primary clinical entity.

Background: Primary cranio-cervical dystonia (PCCD) is an idiopathic condition, which typically occurs in late adulthood and in women more than men. Primary tics (PT) generally start during childhood/adolescence, and a later age of onset or other associated movement disorders are “red flags” to suspect secondary causes. Primary dystonia and PT are distinct entities, but nevertheless, a clinical syndrome with these two features has been described. We report a series of patients presenting both PCCD and PT.

Methods: 248 patients with PCCD attending our Botulinum toxin clinic at the National Hospital of Neurology and Neurosurgery – Queen Square, were examined for PT over a period of 4 months. Secondary tic causes were excluded by clinical interview and appropriate investigations (brain MRI, extensive blood tests, acanthocytes, genetics).

Results: We have found 16 patients (6,5%) with PCCD, also presenting PT. Thirteen patients are males while three are females. In eleven dystonia started below the age of 40. Eleven had a focal involvement, while 5 a segmental. Dystonia was found to affect neck (13), vocal cords (4), jaw (1) eyes (1) and arms (4). Six patients displayed a sensory trick. The association with tics can be stratified as follows: 3/16 patients presented tics before 21 years old, fitting Tourette’s syndrome (GTS) criteria (also presenting >1 motor tic and ≥1 vocal tic); for the other patients, we were not able to recall the onset, which was therefore more likely to fall into the Adult Primary Tics (APT) category. Most of our patients also showed psychiatric issues (hyperactivity, anxiety, depression or obsessive-compulsive features), which were generally mild.

Conclusions: We described a primary clinical entity of PCCD associated with PT. This syndrome differs from pure cranio-cervical dystonia by a higher prevalence in males and a lower age of onset. It presents a tic disorder, which, in a minority of cases resembles GTS, whereas more frequently falls into APT category.

References: Damasio J, Edwards MJ, Alonso-Canovas A, Schwingenschuh P, Kagi G and Bhatia KP. The Clinical Syndrome of Primary Tic Disorder Associated with Dystonia: A Large Clinical Series and a Review of the Literature, Movement Disorders, Vol. 26, No. 4, 2011. Stone LA and Jankovic J. The coexistence of tics and dystonia. Arch Neurol 1991;48:862–865.

To cite this abstract in AMA style:

C. Del Gamba, A. Latorre, U. Bonuccelli, R. Ceravolo, K. Bhatia. The association of primary dystonia with tics – chance or new syndrome? [abstract]. Mov Disord. 2018; 33 (suppl 2). https://www.mdsabstracts.org/abstract/the-association-of-primary-dystonia-with-tics-chance-or-new-syndrome/. Accessed June 14, 2025.
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