Influence of family history on clinical expression of Tourette's syndrome

Neurology ◽  
1999 ◽  
Vol 52 (2) ◽  
pp. 308-308 ◽  
Author(s):  
D. G. Lichter ◽  
J. Dmochowski ◽  
L. A. Jackson ◽  
K. S. Trinidad
Author(s):  
M. Gonce ◽  
A. Barbeau

SUMMARY:The histories of seven consecutive cases of Gilles de la Tourette's syndrome are presented to exemplify the range of clinical manifestations in this disease and to collate preliminary results with the new benzodiazepine, clonazepam, as a possible adjuvant therapy of this disorder. Controlled trials with clonazepam alone and in association with haloperidol are now justified. Five of our 7 patients had a positive family history of tics, and 2 a confirmed family history of gout. Because clonazepam improves myoclonia and tics and because its mechanism of action possibly involves serotonin, we thought it worthwhile to study simultaneously the relative roles of serotonin and dopamine metabolism in the production of tics, and their relationship to possible defects in purine metabolism in Gilles de la Tourette's syndrome.


1970 ◽  
Vol 4 (3) ◽  
pp. 155-158 ◽  
Author(s):  
M. H. De Groot ◽  
Betty Bardwell

The rare syndrome of compulsive swearing and tics, named after Georges Gilles de la Tourette, has been recorded previously in the Southern Hemisphere, although these records have been overlooked in many reviews. The case history of a 17-year-old New Zealand boy is reported. In this case, there is a marked family history of schizophrenia. Some of the features of this patient are discussed.


1998 ◽  
Vol 28 (3) ◽  
pp. 341-351 ◽  
Author(s):  
Humberto C. Párraga ◽  
Marianela I. Párraga ◽  
Laura R. Spinner ◽  
Desmond P. Kelly ◽  
Suzanne L. Morgan

Objective: As many as 35 percent of Tourette's Syndrome patients do not acquire this disorder genetically. Since there has been little research conducted in this area, the purpose of this study was to compare the clinical differences between two groups of patients with Tourette's Syndrome (TS), one with family history of TS and one without. Method: Using data of eight previously diagnosed TS patients, the authors made comparisons of clinical and sociodemographic variables between a group of three patients with family history of TS and five with no family history. Results: There were no differences in clinical presentation, current age, age at diagnosis, gender, and socioeconomic status. There were differences in birth history, developmental milestones, I.Q., and neurological findings between patients with family history and no family history of TS. Conclusions: Our findings support the need for testing the hypothesis of a multidetermined origin of TS, a disorder in which hereditary, neuropsychological, and environmental factors play a role.


1996 ◽  
Vol 41 (1) ◽  
pp. 81-81
Author(s):  
Terri Gullickson ◽  
Pamela Ramser

2001 ◽  
Author(s):  
M. A. Clarke ◽  
M. A. Bray ◽  
T. J. Kehle ◽  
S. D. Truscott

1992 ◽  
Vol 15 (1) ◽  
pp. 109-129 ◽  
Author(s):  
Donald J. Cohen ◽  
Mark A. Riddle ◽  
James F. Leckman

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