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Neurologic aspects of spasmodic dysphonia
D B Rosenfield1, D T Donovan, M Sulek
1Department of Neurology, Baylor College of Medicine, Houston, Texas 77030.
The Journal of Otolaryngology
|August 1, 1990
Summary
Spasmodic dysphonia often stems from organic neurological conditions. Many patients exhibit underlying essential tremor or Meige's syndrome, indicating a neurological basis for their voice disorder.
Area of Science:
- Neurology
- Otolaryngology
- Speech-Language Pathology
Background:
- Spasmodic dysphonia (SD) is a voice disorder characterized by involuntary muscle spasms in the larynx.
- The precise etiology of SD remains incompletely understood, with various contributing factors proposed.
- Understanding the underlying causes is crucial for effective diagnosis and treatment of SD.
Purpose of the Study:
- To investigate the etiological factors in a cohort of 100 patients diagnosed with spasmodic dysphonia.
- To identify the prevalence of specific neurological and functional conditions associated with SD.
- To determine the extent to which organic neurolaryngeal disease contributes to SD.
Main Methods:
- Retrospective analysis of medical records for 100 patients with spasmodic dysphonia.
- Categorization of patients based on diagnosed underlying conditions, including essential tremor, Meige's syndrome, hypothyroidism, functional disturbance, and focal dystonia.
- Clinical assessment and diagnostic workup for each patient.
Main Results:
- A significant majority of patients (71) had underlying essential tremor.
- Other identified causes included Meige's syndrome (25 patients), hypothyroidism (12 patients), and functional disturbance or focal dystonia (27 patients).
- Six patients presented with intermittent breathy dysphonia, suggesting varied clinical presentations.
Conclusions:
- A substantial proportion of spasmodic dysphonia cases are linked to identifiable organic neurolaryngeal diseases.
- Essential tremor and Meige's syndrome are common comorbidities in patients with spasmodic dysphonia.
- These findings underscore the importance of comprehensive neurological and etiological evaluation in SD patients.