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Response of spinal myoclonus to a combination therapy of autogenic training and biofeedback
INTRODUCTION: Clinical evidence indicates that certain types of movement disorders are due to psychosomatic factors. Patients with myoclonic movements are usually treated by a variety of therapeutic agents. Autogenic training (AT), a recognized form of psychosomatic therapies, is suitable for certai...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173903/ https://www.ncbi.nlm.nih.gov/pubmed/17931427 http://dx.doi.org/10.1186/1751-0759-1-18 |
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author | Sugimoto, Koreaki Theoharides, Theoharis C Kempuraj, Duraisamy Conti, Pio |
author_facet | Sugimoto, Koreaki Theoharides, Theoharis C Kempuraj, Duraisamy Conti, Pio |
author_sort | Sugimoto, Koreaki |
collection | PubMed |
description | INTRODUCTION: Clinical evidence indicates that certain types of movement disorders are due to psychosomatic factors. Patients with myoclonic movements are usually treated by a variety of therapeutic agents. Autogenic training (AT), a recognized form of psychosomatic therapies, is suitable for certain types of neurological diseases. We describe a patient with myoclonus who failed to respond to conventional medical therapy. His symptoms were exaggerated by psychogenic factors, especially anger. CASE PRESENTATION: A 42-year-old man was admitted to our hospital, Preventive Welfare Clinic, for severe paroxysmal axial myoclonus of the left shoulder and abdominal muscles. The initial diagnosis was "combination of spinal segmental myoclonus and propriospinal myoclonus". The myoclonic movements did not occur during sleep but were aggravated by bathing, alcohol drinking, and anger. Psychological examination indicated hostile attribution. Although considered not to be a case of psychogenic myoclonus, a "psychogenic factor" was definitely involved in the induction of the organic myoclonus. The final diagnosis was "combination of spinal segmental myoclonus and propriospinal myoclonus accompanied by features of psychosomatic disorders". The patient underwent psychosomatic therapy including AT and surface electromyography (EMG)-biofeedback therapy and treatment with clonazepam and carbamazepine. RESULTS: AT and EMG-biofeedback resulted in shortening the duration and reducing the amplitude and frequency of the myoclonic discharges. CONCLUSION: Psychosomatic therapy with AT and surface EMG-biofeedback produced excellent improvement of myoclonic movements and allowed the reduction of the dosage of conventional medications. |
format | Text |
id | pubmed-2173903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-21739032008-01-03 Response of spinal myoclonus to a combination therapy of autogenic training and biofeedback Sugimoto, Koreaki Theoharides, Theoharis C Kempuraj, Duraisamy Conti, Pio Biopsychosoc Med Case Study INTRODUCTION: Clinical evidence indicates that certain types of movement disorders are due to psychosomatic factors. Patients with myoclonic movements are usually treated by a variety of therapeutic agents. Autogenic training (AT), a recognized form of psychosomatic therapies, is suitable for certain types of neurological diseases. We describe a patient with myoclonus who failed to respond to conventional medical therapy. His symptoms were exaggerated by psychogenic factors, especially anger. CASE PRESENTATION: A 42-year-old man was admitted to our hospital, Preventive Welfare Clinic, for severe paroxysmal axial myoclonus of the left shoulder and abdominal muscles. The initial diagnosis was "combination of spinal segmental myoclonus and propriospinal myoclonus". The myoclonic movements did not occur during sleep but were aggravated by bathing, alcohol drinking, and anger. Psychological examination indicated hostile attribution. Although considered not to be a case of psychogenic myoclonus, a "psychogenic factor" was definitely involved in the induction of the organic myoclonus. The final diagnosis was "combination of spinal segmental myoclonus and propriospinal myoclonus accompanied by features of psychosomatic disorders". The patient underwent psychosomatic therapy including AT and surface electromyography (EMG)-biofeedback therapy and treatment with clonazepam and carbamazepine. RESULTS: AT and EMG-biofeedback resulted in shortening the duration and reducing the amplitude and frequency of the myoclonic discharges. CONCLUSION: Psychosomatic therapy with AT and surface EMG-biofeedback produced excellent improvement of myoclonic movements and allowed the reduction of the dosage of conventional medications. BioMed Central 2007-10-12 /pmc/articles/PMC2173903/ /pubmed/17931427 http://dx.doi.org/10.1186/1751-0759-1-18 Text en Copyright © 2007 Sugimoto et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Study Sugimoto, Koreaki Theoharides, Theoharis C Kempuraj, Duraisamy Conti, Pio Response of spinal myoclonus to a combination therapy of autogenic training and biofeedback |
title | Response of spinal myoclonus to a combination therapy of autogenic training and biofeedback |
title_full | Response of spinal myoclonus to a combination therapy of autogenic training and biofeedback |
title_fullStr | Response of spinal myoclonus to a combination therapy of autogenic training and biofeedback |
title_full_unstemmed | Response of spinal myoclonus to a combination therapy of autogenic training and biofeedback |
title_short | Response of spinal myoclonus to a combination therapy of autogenic training and biofeedback |
title_sort | response of spinal myoclonus to a combination therapy of autogenic training and biofeedback |
topic | Case Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173903/ https://www.ncbi.nlm.nih.gov/pubmed/17931427 http://dx.doi.org/10.1186/1751-0759-1-18 |
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