Abstract

Gilles de la Tourette syndrome (GTS) is characterized by multiple motor and vocal tics. Adult-onset cases are rare and may be due to “reactivation” of childhood tics, or secondary to psychiatric or genetic diseases, or due to central nervous system lesions of different etiologies. Late-onset psychogenic motor/vocal tics resembling GTS have been described. Neurophysiology may serve to differentiate organic from functional GTS. Altered blink reflex pre-pulse inhibition (BR-PPI), blink reflex excitability recovery (BR-ERC), and short-interval intracortical inhibition (SICI) have been described in GTS. We report a 48-years-old male, who developed numerous motor/vocal tics 2 months after sustaining non-commotional craniofacial trauma in a car accident. Both his father and brother had died earlier in car crashes. He presented with blepharospasm-like forced lid closure, forceful lip pursing, noisy suction movements, and deep moaning sounds, occurring in variable combinations, without warning symptoms or internal “urge.” Tics showed low distractibility and these increased with attention. Standard magnetic resonance imaging, electroencephalography, and evoked potentials were unremarkable. Neuropsychology diagnosed moderately impaired intellect, attention, and executive functions. Psychiatric assessment revealed somatization disorder and generalized anxiety. BR-PPI was unremarkable, while BR-ERC was enhanced, even showing facilitation at short intervals. SICI was markedly reduced at 1 and 3 ms and intracortical facilitation (ICF) was enhanced at 10 ms. The patient fulfilled Fahn and Williams' diagnostic criteria for a psychogenic movement disorder. Neurophysiology, however, documented hyperexcitability of motor cortex and brainstem. We suggest that—similar to what has been reported in psychogenic dystonia—a pre-existing predisposition may have led to the functional hyperkinetic disorder in response to severe psychic stress.

Highlights

  • Gilles de la Tourette syndrome (GTS), first reported in 1885 by the homonymous French physician [1], is a neurodevelopmental disorder characterized by multiple motor and vocal/phonic tics in variable combination, with typical copro- and echophenomena

  • We report a patient with borderline intellectual functioning who developed facial motor and phonic tics shortly after a car accident causing a non-commotional head injury

  • An abnormally enhanced blink reflex excitability recovery (BR-ERC) has been reported in GTS and has allowed distinguishing essential from psychogenic blepharospasm [25]

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Summary

Introduction

Gilles de la Tourette syndrome (GTS), first reported in 1885 by the homonymous French physician [1], is a neurodevelopmental disorder characterized by multiple motor and vocal/phonic tics in variable combination, with typical copro- and echophenomena. Due to the non-univocal diagnostic classification of the patient’s symptoms and in order to rule out neuronal dysfunction despite normal imaging studies, several neurophysiological examinations were carried out in this patient so as to investigate excitatory and inhibitory trigemino-facial circuits within the brainstem and to assess inhibitory circuits of the primary motor cortex.

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