Gait, Cerebellar Function, and Movement Disorders Flashcards

1
Q

what helps provide coordination and postural control of gait

A

cerebellar and EPS

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2
Q

gait apraxia

A

have adequate strength, coordination, postural control, and sensation to walk but are immobile when asked to do so

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3
Q

Romberg sign

A

-suggests a problem with impaired proprioception, either from involvement of posterior or dorsal column pathway or their afferent sensory nerves

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4
Q

broad based ataxic gait

A

lesions in posterior columns or proprioceptive sensory nerves OR cerebellar dysfunction

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5
Q

hemiplegic gait

A
  • stroke pts
  • affected lower limb stiffly extended and swung when walking
  • ipsi upper limb flexed at elbow and wrist with decreased armswing
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6
Q

tabetic gait

A

foot slapping

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7
Q

steppage gait

A
  • pts with foot drop of weak dorsiflexion of the foot
  • unilat: lesion in peroneal nerve or L5 root
  • bilat: severe polyneuropathy, motor neuron dz, or b/l L5 lesions
  • hip is flexed and pulled up even higher to elevate drooping foot
  • distal sensory loss and weakness
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8
Q

duck waddle/waddling gait

A

-2/2 weakness of hip girdle, seen in myopathy (muscle dz)

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9
Q

scissors gait

A
  • 2/2 UMN (Corticospinal tract) lesions affecting the lower limbs, as in spastic paresis
  • increased spastic tone and tightness in adductor muscles of thigh force the lower limbs together when walking
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10
Q

parkinsonian gait

A

slow and shuffling, dec armswing, stooped forward/bent over

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11
Q

cerebellar function

A

helps maintain the smoothness and precision of movements for the limbs, trunk, eyes, and voice

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12
Q

What tests are used to identify cerebellar function?

A
  • finger nose finger
  • heel shin knee
  • rapid alternating movements
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13
Q

dysdiadochokinesia

A

uncoordinated, nonrhythmic, sloppy hand movements 2/2 cerebellar dysfunction

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14
Q

rebound phenomenon/abnml check reflex

A
  • imbalance between agonist and antagonist muscles

- pt accidentally strikes face

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15
Q

cerebellar dysarthria

A

-slurred speech associated with involvement of left cerebellar hemisphere

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16
Q

nystagmus

A

-multidirectional, can be due to: cerebellar dz (but also: lesions of vestibular system and brain stem)

17
Q

What does a lesion of a cerbellar hemisphere predominantly affect

A

IPSI limbs; causing:

  • kinetic tremor
  • limb dysmetria
  • dysdiadochokinesia
  • rebound phenomenon
18
Q

what part of the body is affected by a midline lesion of the cerebellar vermis?

A

the TRUNK=truncal unsteadiness when walking/standing, with impaired balance and gait ataxia

19
Q

alcoholic cerebellar degeneration

A
  • toxic disorder
  • chronically leads to atrophy of anterior-superior vermis (area of trunk and lower limbs)
  • deficits include: gait ataxia, truncal unsteadiness, lower limb dysmetria
20
Q

Friedreich’s ataxia

A
  • spinocerebellar degeneration
  • aut recessive
  • spinocerebellar tract lesions (w/ patchy loss of cerebellar Purkinje cells)=limb dysmetria, gait ataxia, dysarthria
  • corticospinal tract lesions=weakness and Babinski signs
  • lesions of drg and dorsal of posterior columns affects lower limbs, causing l/o vibration, position sense, and absent reflexes
21
Q

What are non neurologic features of F’s ataxia

A
  • scoliosis
  • pes cavus (high arched feet)
  • cardiac hypertrophy
  • potentially fatal cardiac arrhythmias
22
Q

How is a clinical diagnosis of F’s ataxia made

A

blood test revealing multiple trinucleotide repeats from a defect in chromosome 9

23
Q

What kind of tremor is typical of PD

A

resting tremor of the limbs or head-noticeable during rest

24
Q

postural tremor

A

more noticeable when limbs maintained in various positions-holding object or extending arm/leg
-often d/t familial essential tremor

25
Q

kinetic tremor

A

-in a limb moving towards a target or performing a task; may accompany other s/s of cerebellar dz

26
Q

choreoathetosis

A
  • athetosis: slow writhing continuous mvmt of distal limbs
  • chorea: purposeless random mvmt of limbs, face, neck, trunk
  • 2/2 lesions in caudate nucleus or its connecting pathways
  • **Huntington’s dz
27
Q

hemiballismus

A
  • violent rapid flinging mvmt of proximal limbs on one side

- 2/2 lesion in contralat subthalamic nucleus

28
Q

dystonia

A
  • continued painful contraction of muscles leading to spasms; unnatural fixed postures
  • focal (cervical dystonia/torticollis) or generalized
29
Q

tics

A
  • brief repetitive focal muscle contractions

- ??d/t decreased motor inhibition in basal ganglia??

30
Q

Tourette’s syndrome

A

-boys, assoc with ADHD–motor tics + vocal tics

31
Q

Which movement disorders accompany encephalopathy

A

myoclonus (myoclonic jerks) and asterixis

32
Q

myoclonus

A

rapid shocklike lightening movements or jerks of limbs and trunk

33
Q

asterixis

A

extended hands and feet, flapping tremor

34
Q

tx resting tremor of PD

A

anticholinergic drugs

35
Q

tx essential tremor

A

beta adrenergic blockers or barbiturates

36
Q

what are dopamine antagonist drugs used to tx

A
  • choreoathetosis
  • hemiballismus
  • tics
37
Q

tx for dystonia

A
  • anticholinergic drugs
  • benzos
  • botulinum toxin injections into the affected muscles
38
Q

deep brain stimulators

A
  • inhibit the thalamus for essential tremor

- inhibit STN for PD

39
Q

resting Pill rolling tremor

A

-low amplitude, low freq
-starts in one hand may progress to involve other extremities, jaw, face, tongue, lips
(PD d/t loss of DA neurons in basal ganglia)