Examination of coordination and gait Flashcards

1
Q

give an example of a dementing disease

A

Alzheimer’s disease

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2
Q

give an example of a movement disorder

A

Parkinson’s disease

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3
Q

Give an example of a motor neuron disease

A

ALS

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4
Q

What are EPS signs indicative of basal ganglia disorder?

A

resting tremor, hypokinesis (rigidity/bradykinesia), hyperkinesis (chorea/athetosis/akathesia)

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5
Q

What are EPS signs of cerebellar disorders?

A

Ataxia (3D’s), dysequilibrium, hypotonia, action tremor, nystagmus

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6
Q

What distinguishes pyramidal dysfunction from EPS?

A

pyramidal: arises from cortex/corticospinal tract –> WEAKNESS. Dysfunction of voluntary movement

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7
Q

describe hemiparetic gait

A

Patient holds one arm to the side, drags affected leg in semicircle. Weakness of distal muscles, extensor hypertonia in lower limb. UMN injury (eg; hemispheric stroke)

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8
Q

describe diplegic gait

A

walking with abnormally narrow base, dragging legs and scraping toes. Spasticity in lower extremities > upper extremities. Seen with bilateral periventricular lesions (cerebral palsy)

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9
Q

describe neuropathic gait

A

aka: equine gait. weak dorsiflexion –> pt must lift leg high so foot doesn’t drag while walking.
Unilateral: peroneal nerve palsy, L5 radiculopathy.
Bilateral: ALS, Charcot-Marie-Tooth, uncontrolled diabetes

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10
Q

describe myopathic gait

A

aka: waddling gait.
unilateral hip girdle weakness –> drop in pelvis on contralateral side while walking (Trendelenburg sign).
Bilateral weakness –> pelvis drops on both sides –> waddling
Seen in myopathies (muscular dystrophy)

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11
Q

Describe bradykinetic gait

A

aka: Parkinsonian gait. Walks with stooped posture, knee flexion, slow and small steps. Seen in Parkinson’s

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12
Q

Choreiform gait

A

aka: hyperkinetic gait
Irregular, jerky, involuntary movements in all extremities
Seen in Hungtington’s disease

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13
Q

Ataxic gait

A

Clumsy, staggering movements with wide-based gait. Standing still –> body swinging back and forth, side-to-side (titubation)
Seen in: cerebellar disease, acute alcohol intoxication, cerebellar vermis disease (truncal instability)

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14
Q

Sensory gait

A

loss of proprioceptive input when feet touch the ground –> patient slams foot to sense the ground. Exacerbated in the dark.
Seen in dorsal column disorders (B12 deficiency/tabes dorsalis) and peripheral nerve dysfunction (uncontrolled diabetes)

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15
Q

What are the pathological characteristics of Multiple System atrophy

A

oligodendroglial alpha synuclein-immunoreactive inclusions in limbic system, brainstem, and/or basal ganglia

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16
Q

Describe Shy-Drager syndrome

A

Multiple System atrophy involving Intermediolateral column degeneration and gliosis. Alpha-synuclein-immunoreactive argyrophilic glial cytoplasmic inclusions

17
Q

What are the three primary “tauopathies”?

A

Alzheimer’s disease, Frontal lobe degeneration of non-Alzheimer type, and Pick disease

18
Q

What tauopathies are associated with EPS?

A

Progressive supranuclear palsy (PSP) and Cortical Basal Degeneration (CBD)

19
Q

What are the primary characteristics of Progressive Supranuclear Palsy?

A

akinesia, rigidity, characteristic supranuclear gaze palsy

20
Q

What are the primary characteristics of Corticobasal degeneration?

A

initially clumsy and stiff, later rigid and akinetic

21
Q

What are the pathological characteristics of Huntington’s disease?

A

progressive atrophy of neostriatum (anterior caudate and dorsal putamen)

22
Q

What are the genetic characteristics of Friederich’s ataxia?

A

autosomal recessive. Chromosome 9q. GAA repeat expansion –> mitochondria dysfunction

23
Q

How does Friedreich’s ataxia manifest clinically?

A

limb ataxia, dysarthria, loss of distal position and vibration sense, upper limb wasting