Cerebellar Disorders Flashcards
Cerebellar Disorders Movement System Diagnoses
Movement Pattern Coordination Deficit
Dysmetria
Cerebellar Disorders Prognosis
Better
- Metabolic causes
- Static, small focal lesions - MS
- Trunk ataxia
- Ischemic stroke
- PICA or AICA
- No CB nuclei involvement
Worse
- Degenerative diseases
- Multiple, large focal lesions - MS
- Limb ataxia
- Hemorrhagic stroke
- SCA
- CB nuclei involvement
Vertebral & PICA Stroke Signs & Symptoms
Vertigo
Nausea
Hoarsness
Dysphagia
Ipsilateral ataxia
Ptosis
Impaired sensation of the ipsilateral face and contralateral torso & limbs
Autosomal dominant cerebellar disorders
Spinocerebellar ataxias
Midlife onset
Slowly progressive
Autosomal recessive cerebellar disorders
Friedreich ataxia
Onset 5-15yo - 15% get symptoms after 25
10-20y before confined to a wheelchair
Individuals completely incapacitated in later stages
Life expectancy shortened from heart complications
Ataxia S&S
Lack of coordination
Slurred speech
Trouble eating
Trouble swallowing
Eye movement
Fine motor skill deterioration
Difficulty ambulating
Gait deviation
Tremors
Heart problems
Dysfunction of voluntary movement signs & symptoms
Dyssynergia & dysmetria of ocular motion & limb movements
Dysdiadochokinesia
Lack of check
Movement decomposition
Postural control & balance deficits
Gait ataxia
Hypotonia
Low muscle tone
Cerebellar tremors
Action tremor that is slow velocity high amplitude
Postural tremor
Kinetic tremor - intention
Nystagmus
Uncontrolled repetitive eye movements
Can be spontaneous or gaze-evoked
Cerebellar disorders diagnosis-specific tests & measures
Scale for Assessment and Rating of Ataxia (SARA)
International Cooperative Ataxia Rating Scale (ICARS)
Brief Ataxia Rating Scale (BARS)
Friedrich Ataxia Rating Scales (FARS)
Composite Cerebellar Functional Severity (CCFS)
Action Research Arm Test (ARAT)
Cerebellar Disorders Health condition & BSF Impairments
Spinocerebellar ataxias
Freidreich’s Ataxia
Poor timing, sequencing, and consistency of movement
Difficulty with intersegmental movement
Difficulty with anticipatory and reactive postural responses
Difficulty with motor learning
Difficulty grading forces & scaling movements
Cerebellar Disorders Interventions
Coordination training
Proximal stability/ trunk strengthening
Fall prevention & fall strategies
Endurance exercise with medical clearance
Explicit motor control strategies
Cerebellar Disorders Special considerations
Cardiac complications are common
Speech deficits are common
SCAs have an increase in CAG triplets producing a protein that leads to neuronal death and CB degeneration
Friedreich’s ataxia is the most common autosomal recessive hereditary ataxia
Dysarthria
Scanning speech/Ataxic dysarthria
- spoken words are broken up into separate syllables, often separated by noticeable pauses and spoken with varying force
Dyssynergia
impairment of multi-joint movement related to dysmetria and deficits in limb dynamics predictions
Dysdiadochokinesia
deficits in coordinating agonist-antagonist muscle pairs, elicited during rapid alternating movements/rapid reversals
Dysmetria
the impaired ability to scale movement distance; slow movements tend to produce hypometria and fast movements tend to produce hypermetria
Movement decomposition
breaking down of a movement sequence or multi-joint movement into a series of separate movements to simplify the movement
(this may actually represent a compensatory strategy)
Lack of Check
inability to halt unintended movement (excessive rebound)