Definition and Classification of Involuntary Movements

2020 ◽  
pp. 1-6
Author(s):  
Hiroshi Shibasaki ◽  
Mark Hallett ◽  
Kailash P. Bhatia ◽  
Stephen G. Reich ◽  
Bettina Balint

Involuntary movements, also called hyperkinetic movement disorders, are defined as abnormal, unintended movements. They are defined as “abnormal” because not all unintended movements are pathological (reflexive or spontaneous movements also occur but are part of normal function; these include breathing, yawning, blinking, and the like). Involuntary movements can be classified into several categories according to their phenomenological characteristics and then according to the etiology and/or pathophysiology for each kind of involuntary movement. Involuntary movements include tremor, chorea, ballism, athetosis, dystonia, myoclonus, dyskinesia, tics, asterixis, and motor stereotypy. Many of the involuntary movements can occur as side effects of pharmaceutical drugs. Functional or psychogenic involuntary movements are not infrequently encountered.

2013 ◽  
Author(s):  
Kiichi Hirota

Involuntary movement during and after neuraxial anesthesia, such as spinal and epidural anesthesia, is rarely observed. In this report, we describe a case of myoclonus-like involuntary movement of the upper extremities in a patient undergoing a planned repeat cesarean section under spinal anesthesia with bupivacaine that completely subsided after 2mg midazolam administration. The myoclonus-like movement never recurred or caused any apparent neurological side effects. No abnormal sensation or spontaneous pain of the upper extremities was observed. The patient was discharged on foot on post-operative day 3.


Author(s):  
Hiroshi Shibasaki ◽  
Mark Hallett ◽  
Kailash P Bhatia ◽  
Stephen G. Reich ◽  
Bettina Balint

This book is aimed at describing clinical features of various kinds of involuntary movements by demonstrating a number of cases on video. Most of the video cases presented in this book were directly observed and studied by at least one of the five authors, and a few cases were from the published paper with permission. The authors also discuss the current consensus about the classification, pathophysiology, and current treatment of each involuntary movement. This book adopts a unique way of looking at movement disorders by considering two aspects of the diagnosis: Axis 1, the phenomenology, and Axis 2, the etiology and/or pathophysiology. The visual appearance of the disorder, as seen on video, is a big part of Axis 1 diagnosis.


2020 ◽  
pp. 155-162
Author(s):  
Hiroshi Shibasaki ◽  
Mark Hallett ◽  
Kailash P. Bhatia ◽  
Stephen G. Reich ◽  
Bettina Balint

Functional movement disorders are any type of movement disorder due to a brain network disorder where normal function is possible. The terminology of functional movement disorders has changed; in the recent past, these disorders were most frequently called psychogenic. Characteristics of functional movements include incongruity with a known type of involuntary movement; inconsistency in the pattern, degree, and distribution during the clinical course; improvement with distraction; and possible psychogenic background. While the movements are said to be fully involuntary, there is often some suggestibility. In the case of unilaterally predominant tremor, if the patient is requested to repeat voluntary movements with the intact or less affected hand at a certain pace, the tremor frequency might be replaced by the frequency of the voluntary movement, the phenomenon called entrainment.


2014 ◽  
Vol 2 (2) ◽  
pp. 224-228
Author(s):  
Andrej N. Ilanković ◽  
Vera Ilanković ◽  
Nikola N. Ilanković

Movement disorders and psychomotor deficiency is highly represented among patients in Schizophrenia – residual type.Our therapeutic work and the results we are herewith presenting, reveal that the psychomotor deficiency by Schizophrenia residual conditions represent new and significant indication fields for specific rehabilitation treatment in psychiatry.Evaluation of efficacy after 6 weeks specific rehabilitation treatment with the Vilan method showed: very satisfactory results in correction of involuntary movements of the torso,   bradykinesia of the hands,  praxia  and the simple simultaneous movements; satisfactory correction of involuntary movements of the extremities, walking  and  the facial gestures. No correction was in: involuntary movement of mouth and face, tremor, ideation, ideo‑motor series and in complex simultaneous movement.


Author(s):  
Nicholas Fletcher

Almost any neurological disorder can produce a disorder of movement but the ‘movement disorders’ include the akinetic rigid syndromes, hyperkinesias, and some tremors. It can sometimes seem, especially with the use of videotape recordings, that diagnosis of movement disorders is mainly a matter of correct visual recognition. Such an approach is not recommended and can lead to mistakes unless, as in other areas of medicine, the history is considered first and the physical signs second. Obvious examples include the family history in Huntington’s disease, developmental history in dystonic cerebral palsy, and neuroleptic drug treatment in patients with tardive dyskinesia. In addition, a single disorder may give rise to several different types of involuntary movement. For example, Huntington’s disease may give rise to an akinetic rigid state, chorea, myoclonus, tics, or dystonia. Patients with Parkinson’s disease taking levodopa may show different types of movement disorder at different times of the day.In akinetic rigid states the diagnostic issue will be whether the patient has idiopathic Parkinson’s disease or one of the other Parkinsonian syndromes. With involuntary movements, the first step in diagnosis is to classify these as dystonia, tics, tremor, chorea, or myoclonus. It must be remembered that involuntary movements are merely physical signs, not diagnostic entities, and that they do not always occur in a pure form; for example, patients with dystonia may have additional choreiform movements or tremor. If more than one form of abnormal movement seems to be present, the diagnosis should be based on the most obvious one. The next step is to decide on the cause of the movements and at this stage the diagnosis must be based upon an accurate and complete history as noted above.The movement disorders are often associated with abnormalities of the basal ganglia and, to some extent, vice versa. This is not entirely correct. Disturbances of basal ganglia function certainly have profound effects on movement with the development of bradykinesia, rigidity, tremor, or the various forms of dyskinesia. However, it is not correct when considering the pathophysiology of movement disorders to regard the basal ganglia as an isolated movement control centre. In fact, they are an important but poorly understood component of a much wider motor system. It is also important to remember that the basal ganglia are involved in the processing of limbic and other cognitive processes which may also be disturbed by basal ganglia dysfunction.


2013 ◽  
Author(s):  
Kiichi Hirota

Involuntary movement during and after neuraxial anesthesia, such as spinal and epidural anesthesia, is rarely observed. In this report, we describe a case of myoclonus-like involuntary movement of the upper extremities in a patient undergoing a planned repeat cesarean section under spinal anesthesia with bupivacaine that completely subsided after 2mg midazolam administration. The myoclonus-like movement never recurred or caused any apparent neurological side effects. No abnormal sensation or spontaneous pain of the upper extremities was observed. The patient was discharged on foot on post-operative day 3.


2020 ◽  
Vol 65 (6) ◽  
pp. 693-704
Author(s):  
Rafik Djemili

AbstractEpilepsy is a persistent neurological disorder impacting over 50 million people around the world. It is characterized by repeated seizures defined as brief episodes of involuntary movement that might entail the human body. Electroencephalography (EEG) signals are usually used for the detection of epileptic seizures. This paper introduces a new feature extraction method for the classification of seizure and seizure-free EEG time segments. The proposed method relies on the empirical mode decomposition (EMD), statistics and autoregressive (AR) parameters. The EMD method decomposes an EEG time segment into a finite set of intrinsic mode functions (IMFs) from which statistical coefficients and autoregressive parameters are computed. Nevertheless, the calculated features could be of high dimension as the number of IMFs increases, the Student’s t-test and the Mann–Whitney U test were thus employed for features ranking in order to withdraw lower significant features. The obtained features have been used for the classification of seizure and seizure-free EEG signals by the application of a feed-forward multilayer perceptron neural network (MLPNN) classifier. Experimental results carried out on the EEG database provided by the University of Bonn, Germany, demonstrated the effectiveness of the proposed method which performance assessed by the classification accuracy (CA) is compared to other existing performances reported in the literature.


2016 ◽  
Vol 214 ◽  
pp. 109-116 ◽  
Author(s):  
Mark Lowrie ◽  
Laurent Garosi

1988 ◽  
Vol 62 (3) ◽  
pp. 979-985 ◽  
Author(s):  
Arthur S. Walters ◽  
Doris Wright ◽  
James Boudwin ◽  
Karl Jones

Three hysterical movement disorders are reported: a case of hysterical bilateral blepharospasm which later presented as hysterical hemifacial spasm, a case of hysterical myoclonus, and a case of hysterical parkinsonism. Two patients presented with a relative indifference to preceding life experiences that would normally have evoked considerable emotion. Two of the cases first presented at an older age and one of these older patients was a man. Two of the patients agreed to hypnotherapy and supportive psychotherapy. In both cases the “involuntary” movements disappeared during hypnosis. In the third case, there was a complete spontaneous resolution of symptoms in a neurological condition where resolution would not be expected to occur.


Basal Ganglia ◽  
2011 ◽  
Vol 1 (2) ◽  
pp. 120-121
Author(s):  
M.O. Pinsker ◽  
F. Amtage ◽  
M. Berger ◽  
G. Nikkhah ◽  
L. Tebartz van Elst

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