Movement Disorders
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jester2357 on November 4, 2010
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48 terms
Terms | Definitions |
|---|---|
Quadraplegia | whole body involved in varying degrees |
Diplegia | whole body involved but LEs>UEs; symmetrical or asymmetrical distribution; good head control and min/mod involement of UEs |
Hemiplegia | one side involved (face, UE, trunk, LE) |
Monoplegia | one extremity involved |
Paraplegia | involvement of trunk and LEs to varying degrees |
Spasticity Presentation | increased muscle tone of muscle groups, increased tension when lengthened, firm/tense on palpation, distribution between flexors and extensors is asymmetrical increased DTR/MSR, increased incrementally with rate/velocity, excitation and position change, clonus, decreased PROM with atypical firm end feel, increased cocontration and decreased reciprocal inhibition, primitive reflexes present, disuse atrophy |
Rigidity Presentation | increased muscle tone of muscle groups,continuous or sometimes intermittent sustained muscle contraction even when appear relaxed, increased tension uniformly and immediately as lengthened, firm/tense on palpation, no change or increase in DTR/MSR, no change with rate/velocity and position, decreased PROM with atypical firm end-feel, distribution between flexors and extensors is equal, increased cocontraction and decreased reciprocal inhibition, disuse atrophy, LEAD-PIPE constant rigidity to movement throughout ROM; COGWHEEL alternative episodes of resistance and relaxation through ROM |
Hypotonicity/Atonia Presentation | decreased muscle tone of groups, decreased tension when lengthened, soft/mushy on palpation, decreased DTR/MSR, possible change with rate/velocity and position, increased PROM with hard or empty end-feel, distribution b/w flexors and extensors usually symmetrical (can be asymmetrical), decreased cocontration and reciprocal inhibition, some tonic reflexes, atrophy, weakness and decreased endurance |
Athetosis Presentation | fluctusting/changeable/unfixed muscle tone, ROM not affected, asymmetrical distribution, may be mixed with spasticity and others, decreased cocontration and increased reciporcal inhabition (particularly extremities), primitive/tonic reflexes present, decreased strength. |
Non-Tension Athetoid | involuntary movements without increase in muscle tone |
Dystonic Athetoid | abnormal posturing of limbs/head/trunk with unpredictable increases in tone |
Choreoathetoid | involuntary, unpredictable small movements of head and distal extremities, some say large, jerky movements. |
Tension Athetoid | increased mm tone which blocks involuntary movement |
Dystonia/Torsion Spasm | fluctuating becoming increased muscle tone that is severe and unrelieving/sustained increased tension with lengthening, tense/firm on palpation, increased DTR/MSR, decreased PROM with firm end-feel, persistent attitude or posture in one or other extremes of athetoid movement, tends to be in large axial muscles, may be mixed with athetosis and others |
Chorea Presentation | decreased muscle tone to fluctuating muscle tone, 'dance' of involuntary arrhythmic movements of a forceful rapid, jerky type, simple or complex patterns of movement purposeless, PROM not as affected, distribution variable, may be mixed with athetosis and others, proximal limb muscles involved in wide range and flinging movements= hemiballisums, chorea of one side of the body= hemichorea |
Ataxia Presentation | low postural tone with occasional changes to above normal, abnormalities of intended movement, dyssynergia/ asynergia/ decompensation, dysmetria, dysdiadochokinesis, intention tremor, titubation, hypermobile, primitive reflexes modified in children but late |
Dysmetria | inability to hit targets, overshooting and undershooting |
Dysdiadochokinesis | inability to rapidly alternate movements; for example, inability torapidly pronate and supinate the forearm or inability to rapidly alternate toe tapping. |
Titubation | a tremor seen in the trunk |
Apraxia Presentation | disturbance of motility in which a clear minded individual with no weakness, spasticity, athetosis, atacia, or other extrapyramidal derangement, and no defects in sensation does not develop or loses the ability to excecute skills and gestures, may see hypotonia |
Ideational Apraxia | failure to conceive or formulate an action spontaneously or on command; inability to perform dynamic, sequencial skill upon request. |
Ideomotor Apraxia | failure to excecute an action despite having knowledge and memory of the planned action; inability to carry out simple, one step task upon request |
Resting Tremor | course, rhythmic tremor of 3-5 Hz, alternating contractions of agonist/antagonist muscles, and amplitude varying with stress/fatigue/medications; seen in hands, forearms, feet, jaw, lips, or tongue when is in an 'attitude of repose': suppressed/lessened with active movement |
Intention Tremor | irregular, mostly rhythmical, 2-3 Hz oscillations in several planes of movement observed during active movements especially those requireing precision or movements done when vision is impaired/blocked; may also see titubation |
Postural and Action Tremor | present in limbs and trunk while actively maintaining a certain position and throughout movement; rhythmic bursts of avtivity occurring synchronously and simultaneously in opposing muscle groups; never at the degree of intention tremors |
Hysterical Tremor | usually seen in one limb, gross in nature, and if retrain involved limb the tremor manifests in other limb; less regular quality, present during activity and repose. |
Asterixes | arrhythmic lapses in sustained posture which allow gravity or muscle elasticity to produce movement followed by patient correction with overshoot. |
Clonus | series of uniphasic/monophasic contractions and relaxations as muscle subjected to sudden sustained stretch; seen in conditions of spasticity |
Myoclonus | shock-like contractions of a group of muscles which are irregular in rhythm and amplitude, mostly asynchronous, and asymmetrical in distribution |
Pathological Startle Syndromes | greatly exaggerated startle reflex and other stimulus induced disorders where startle is predominant |
Spasmodic Torticollis and Cranial-Cervical Spasms | intermittent, arrhythmic, brief or prolonged involuntary spasms of contractions of the facial, jaw, lingual, SCM, trapezius, and other neck muscles. |
Tics and Habit Spasms | habitual movements which range from simple, highly personalized, idiosyncratic mannerisms to repetitive actions when individual becomes tense; sterotypy and irresitibility are main features. |
Spastic Movement Quality | poverty of movement, labored movement, small/limited movements, move in midrange versus endranges, appears to dislike movement; difficulty with mobility level of motor control |
Spastic Quadraplegia Movement Quality | spastic characteristics throughout entire body |
Spastic Diplegia Movement Quality | spastic characteristics and good head control with mild/moderate UE deficits trunk and LE limited movement lacking variety; requires increased effort to move and transition. |
Spastic Hemiplegia Movement Quality | spastic characteristics and integration of sides is lost so movement quality on both sides is incomplete and create a new midline center of the uninvolved side; missed development of controlled symmetry needed to relate sides and top to bottom; poor motor planning. |
Athetosis including Chorea and Dystonia Movement Quality | latency, decreased grading and problems with termination of movement causes difficulty with timing; difficulty controlling midrange and sustaining posture, transitioning between positions, and with eccentric control; 'fixes' for stability and appears 'fearless' during movements. |
Hypotonic Movement Qualities | difficulty with initiating, sustaining and terminating movement and postures, and is fearful of movement, uses phasic burts for activity and ligaments/joints in mechanical lock positions. |
Ataxia Movement Qualitites | difficulty with initiation and cessation, timing/sequencing and grading, and fixation for sustained postural control through movements/transitions; fear/dislikes movement due to lack of control; uses joint structures or vision for 'fixing' and demonstrates poor motor planning; unreliable and uncoordinated balance/postural control responses and spontaneous movement. |
Hyperkinetic Movement Qualities | awkward, clumsy, and difficulties with higher level balance/postural control, mature components of gross motor skills and fine motor skills; hyperkinesis with sensory defensiveness causing limited sensory motor experience and movement dysfunction. |
Spasticity Pathologies | Cerebral Palsy, Tramatic Brain INjury, Rett Syndrome |
Rigidity Pathologies | Parkinson's Disease, Near Drowning, Tuberous Sclerosis |
Hypotonicity Pathologies | Fragile X Syndrome, Prader-Willi Syndrome, Down Syndrome, Cri Du Chat Syndrome |
Athetosis Pathologies | Cerebral Palsy, Lesch-Nyhan Syndrome |
Dystonia/Torsion Spasm Pathologies | Cerebral Palsy, Torsion Dystonia, Dystonia Musculorum Deformans |
Chorea Pathologies | Cerebral Palsy, Huntington Chorea, Syndenham Chorea |
Ataxia Pathologies | Cerebral Palsy, Friedreich's Ataxia, Ataxia Telangectasia, Angelman Syndrome |
Apraxia Pathologies | Developmental Coordination Disorder (DCD) |
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