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Neuromuscular Electrical Stimulation Therapy for Dysphagia Caused by Wilson's Disease
Annals of Rehabilitation Medicine ; : 409-413, 2012.
Article in English | WPRIM | ID: wpr-138766
ABSTRACT
Wilson's disease is an autosomal recessive disorder of abnormal copper metabolism. Although dysphagia is a common complaint of patients with Wilson's disease and pneumonia is an important cause of death in these patients, management of swallowing function has rarely been reported in the context of Wilson's disease. Hence, we report a case of Wilson's disease presenting with dysphagia. A 33-year-old man visited our hospital with a complaint of difficulty in swallowing, since about last 7 years and which had worsened since the last 2-3 months. He was diagnosed with Wilson's disease about 13 years ago. On the initial VFSS, reduced hyoid bone movement, impaired epiglottic movement and moderate amount of residue in the valleculae during the pharyngeal phase were noted. After 10 sessions of neuromuscular electrical stimulation for 1 hour per day, decreased amount of residue was observed in the valleculae during the pharyngeal phase on the follow-up VFSS.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pneumonia / Deglutition Disorders / Electric Stimulation Therapy / Follow-Up Studies / Cause of Death / Copper / Deglutition / Electric Stimulation / Hepatolenticular Degeneration / Hyoid Bone Type of study: Observational study / Prognostic study Limits: Adult / Humans Language: English Journal: Annals of Rehabilitation Medicine Year: 2012 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pneumonia / Deglutition Disorders / Electric Stimulation Therapy / Follow-Up Studies / Cause of Death / Copper / Deglutition / Electric Stimulation / Hepatolenticular Degeneration / Hyoid Bone Type of study: Observational study / Prognostic study Limits: Adult / Humans Language: English Journal: Annals of Rehabilitation Medicine Year: 2012 Type: Article