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Head Tremor in Cervical Dystonia

Published online by Cambridge University Press:  04 August 2016

P.K. Pal
Affiliation:
Neurodegenerative Disorders Centre, Vancouver Hospital & Health Sciences Centre, University of British Columbia, Vancouver, BC, Canada
A. Samii
Affiliation:
Neurodegenerative Disorders Centre, Vancouver Hospital & Health Sciences Centre, University of British Columbia, Vancouver, BC, Canada
M. Schulzer
Affiliation:
Neurodegenerative Disorders Centre, Vancouver Hospital & Health Sciences Centre, University of British Columbia, Vancouver, BC, Canada
E. Mak
Affiliation:
Neurodegenerative Disorders Centre, Vancouver Hospital & Health Sciences Centre, University of British Columbia, Vancouver, BC, Canada
J.K.C. Tsui*
Affiliation:
Neurodegenerative Disorders Centre, Vancouver Hospital & Health Sciences Centre, University of British Columbia, Vancouver, BC, Canada
*
Neurodegenerative Disorders Centre, Vancouver Hospital and Health Sciences Centre, Purdy Pavilion, 2221 Wesbrook Mall, Vancouver, BC, Canada V6T2B5
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Abstract:

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Objective:

To compare the clinical characteristics, natural history, and therapeutic outcome of patients with cervical dystonia (CD) with head tremor (HT+) and without head tremor (HT-).

Methods:

We prospectively evaluated 114 consecutive patients of CD over a 9-month period with a detailed questionnaire. Chi-square and t-tests were employed for statistical analysis.

Results:

Seventy-eight (68.4%) patients had head tremor and 27 of them (34.6%) had tremor as one of the first symptoms. Age at onset of symptoms were similar in HT+ and HT- groups; however there was a higher prevalence in women in the former group (66.7% vs. 41.7%; p=0.01). HT+ patients had more frequent positive family history of essential-like hand/head tremor (21.8% vs. 5.5%; p<0.05), associated neck pain (92.3% vs. 77.8%; p<0.05), and essential-like hand tremor (40% vs. 8.3%; p<0.001). They also appeared to have more frequent history of preceding head/neck trauma (14.1% vs. 8.3%), frequent head rotation (88.5% vs. 69.4%) and antecollis (12.8% vs. 5.5%) but less often head tilt (37.2% vs. 47.2%) and gestes antagonistes (60.2% vs. 75%) than the HT- patients; however these differences were not statistically significant. The frequency of prior psychiatric illnesses, the incidence of dystonias in other parts of the body, frequency of retrocollis and shoulder elevation, and spontaneous remission were similar in the two groups.

Conclusions:

Head tremor is common in CD and is more commonly associated with hand tremor and family history of tremor or other movement disorders. This supports a possible genetic association between CD and essential tremor (ET). Linkage studies are required to evaluate the genetic association between CD and ET.

Type
Original Article
Copyright
Copyright © The Canadian Journal of Neurological 2000

References

REFERENCES

1. Fahn, S, Marsden, CD, Calne, DB. Classification and investigation of dystonia. In: Marsden, CD, Fahn, S, eds. Movement Disorders 2. London: Butterworths, 1987:332358.Google Scholar
2. Brautigam, W. Grundlagen und Erscheinungsweisen des Torticollis spasticus. Verlaufsuntersuchungen bei 25 Kranken. Nervenarzt 1954;25:451462.Google Scholar
3. Chan, J, Mitchell, FB, Fahn, S. Idiopathic cervical dystonia: clinical characteristics. Mov Disord 1991;5:119126.CrossRefGoogle Scholar
4. Couch, JR. Dystonia and tremor in spasmodic torticollis. In: Eldridge, R, Fahn, S, eds. Dystonia. New York: Raven Press, 1976:245258.Google ScholarPubMed
5. Lowenstein, DH, Aminoff, MJ. The clinical course of spasmodic torticollis. Neurology 1988;38:530532.Google Scholar
6. Matthews, WB, Beasley, P, Parry-Jones, W, Garland, G. Spasmodic torticollis: a combined clinical study. J Neurol Neurosurg Psychiatry 1978;41:485492.Google Scholar
7. Naber, D, Weinberger, DR, Bullinger, M, Polsby, M, Chase, TN. Torticollis spasmodicus. Eine Untersuchung zu Symptomatik, Verlauf, Familienanamnese und Psychopathologie. Nervenarzt 1986;57:238243.Google Scholar
8. Nutt, JG, Muenter, MD, Aronson, A, Kurland, LT, Melton, III. Epidemiology of focal and generalized dystonia in Rochester, Minnesota. Mov Disord 1988;3:188194.Google Scholar
9. Rondot, P, Marchand, MP, Dellaotolas, G. Spasmodic torticollis review of 220 patients. Can J Neurol Sci 1991;18:143151.CrossRefGoogle ScholarPubMed
10. van Herwaarden, GMFM, Anten, HWM, Hoogduin, CAL, et al. Idiopathic spasmodic torticollis: a survey of the clinical syndromes and patients’ experiences. Clin Neurol Neurosurg 1994;96:222225.CrossRefGoogle ScholarPubMed
11. Claypool, DW, Duane, DD, Ilstrup, DM, Melton, III. Epidemiology and outcome of cervical dystonia (spasmodic torticollis) in Rochester, Minnesota. Mov Disord 1995;10:608614.Google Scholar
12. Friedman, A, Fahn, S. Spontaneous remissions in spasmodic torticollis. Neurology 1986;36:398400.Google Scholar
13. Gauthier, S. Idiopathic spasmodic torticollis: pathophysiology and treatment. Can J Neurol Sci 1986;13:8890.CrossRefGoogle Scholar
14. Lindeboom, R, de Haan, RJ, Aramideh, M, Brans, JWM, Speelman, JD. Treatment outcomes in cervical dystonia: a clinimetric study. Mov Disord 1996;11:371376.Google Scholar
15. Lorentz, IT, Subramaniam, SS, Yiannikas, C. Treatment of idiopathic spasmodic torticollis with botulinum toxin A: a double-blind study on twenty-three patients. Mov Disord 1991;6:145150.Google Scholar
16. Tsui, JK, Eisen, A, Mak, E, et al. A pilot study on the use of botulinum toxin in spasmodic torticollis. Can J Neurol Sci 1985;12:314316.Google Scholar
17. Tsui, JKC, Eisen, A, Stoessl, AJ, Calne, S, Calne, DB. Double-blind study of botulinum toxin in spasmodic torticollis. Lancet 1986;2:245247.Google Scholar
18. Van Zandijcke, M. Cervical dystonia (spasmodic torticollis): some aspects of the natural history. Acta Neurol Belg 1995;95:210215.Google Scholar
19. Duane, DD, Clark, M, Gottlob, L, Case, JL, LaPointe, LL. The influence of family history on cervical dystonia. Mov Disord 1993;8:413414.(Abstract)Google Scholar
20. Rivest, J, Marsden, CD. Trunk and head tremor as isolated manifestations of dystonia. Mov Disord 1990;5:6065.Google Scholar
21. Lou, J, Jankovic, J. Essential tremor: clinical correlates in 350 patients. Neurology 1991;41:234238.Google Scholar
22. Leube, B, Rudnicki, D, Ratzlaff, T, et al. Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal distribution. Hum Mol Genet 1996;10:16731677.Google Scholar