Cerebellar Disorders Flashcards

1
Q

Cerebellar Disorders Movement System Diagnoses

A

Movement Pattern Coordination Deficit
Dysmetria

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2
Q

Cerebellar Disorders Prognosis

A

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

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3
Q

Vertebral & PICA Stroke Signs & Symptoms

A

Vertigo
Nausea
Hoarsness
Dysphagia
Ipsilateral ataxia
Ptosis
Impaired sensation of the ipsilateral face and contralateral torso & limbs

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4
Q

Autosomal dominant cerebellar disorders

A

Spinocerebellar ataxias
Midlife onset
Slowly progressive

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5
Q

Autosomal recessive cerebellar disorders

A

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

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6
Q

Ataxia S&S

A

Lack of coordination
Slurred speech
Trouble eating
Trouble swallowing
Eye movement
Fine motor skill deterioration
Difficulty ambulating
Gait deviation
Tremors
Heart problems

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7
Q

Dysfunction of voluntary movement signs & symptoms

A

Dyssynergia & dysmetria of ocular motion & limb movements
Dysdiadochokinesia
Lack of check
Movement decomposition
Postural control & balance deficits
Gait ataxia

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8
Q

Hypotonia

A

Low muscle tone

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9
Q

Cerebellar tremors

A

Action tremor that is slow velocity high amplitude
Postural tremor
Kinetic tremor - intention

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10
Q

Nystagmus

A

Uncontrolled repetitive eye movements
Can be spontaneous or gaze-evoked

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11
Q

Cerebellar disorders diagnosis-specific tests & measures

A

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)

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12
Q

Cerebellar Disorders Health condition & BSF Impairments

A

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

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13
Q

Cerebellar Disorders Interventions

A

Coordination training
Proximal stability/ trunk strengthening
Fall prevention & fall strategies
Endurance exercise with medical clearance
Explicit motor control strategies

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14
Q

Cerebellar Disorders Special considerations

A

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

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15
Q

Dysarthria

A

Scanning speech/Ataxic dysarthria
- spoken words are broken up into separate syllables, often separated by noticeable pauses and spoken with varying force

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16
Q

Dyssynergia

A

impairment of multi-joint movement related to dysmetria and deficits in limb dynamics predictions

17
Q

Dysdiadochokinesia

A

deficits in coordinating agonist-antagonist muscle pairs, elicited during rapid alternating movements/rapid reversals

18
Q

Dysmetria

A

the impaired ability to scale movement distance; slow movements tend to produce hypometria and fast movements tend to produce hypermetria

19
Q

Movement decomposition

A

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)

20
Q

Lack of Check

A

inability to halt unintended movement (excessive rebound)