Gait, Cerebellar Function, and Movement Disorders Flashcards

1
Q

systems that provide coordination and postural control of gait

A

cerebellar and extrapyramidal systems

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2
Q

can’t walk when asked

A

gait apraxia

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3
Q

Romberg sign - issue with

A

proprioception - dorsal column or afferent sensory nerves

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4
Q

proprioception/sensation is needed for walking when?

A

in dark

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5
Q

broad based ataxic gait

A

posterior column lesion

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6
Q

hemiplegic gait

A

circumducting (ipsi upper limb flexes at elbow too) - stroke patients

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7
Q

tabetic gait

A

foot slap

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8
Q

steppage gait

A

foot drop or weak dorsiflexion

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9
Q

unilateral foot drop

A

peroneal n or L5 root lesion

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10
Q

b/l foot drop

A

polyneuropathy, motor neuron dz, b/l L5 root lesions

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11
Q

waddling gait

A

weakness of hip girdle muscles - myopathy

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12
Q

scissors gait

A

UMN (CST) lesions like spastic paraparesis

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13
Q

parkinsonian gait

A

slow and shuffling with festination (lean forward and inc speed)

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14
Q

overshooting or undershooting target during cerebellar tests

A

dysmetria

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15
Q

uncoordinated nonrhythmic sloppy hand movements instead of rapid/alternating

A

dysdiadochokinesia

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16
Q

kinetic/action tremor due to issue where?

A

cerebellum issue

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17
Q

imbalance between agonist and antagonist muscles

A

rebound phenomenon (ex: pull on dr’s arm but they let go and you can’t stop your arm from moving so you hit yourself)

18
Q

broken down syllables with unequal emphasis/force, jerky speech

A

cerebellar dysarthria

19
Q

multidirectional nystagmus seen w/

A

cerebellar dz, vestibular lesions, brainstem lesions

20
Q

atrophy of anterior-superior vermis - gait ataxia, truncal unsteadiness, lower limb dysmetria - seen with

A

alcoholic cerebellar degeneration

21
Q

autosomal recessive dz that starts in kids and worsens, cerebellum is affected

A

Friedrich’s ataxia - chromosome 9 trinucleotide repeats

22
Q

limb dysmetria, gait ataxia, dysarthria seen w/ lesion where

A

spinocerebellar lesion

23
Q

weakness and babinski sign seen w/ lesion where

A

CST lesion

24
Q

postural tremor seen with

A

familial essential tremor

25
Q

kinetic tremor seen with

A

cerebellar dz

26
Q

continuous slow writhing movements of distal limbs

A

athetosis

27
Q

dance-like irregular movements

A

choreoathetosis

28
Q

unilateral rapid violent flinging movements of proximal limb

A

hemiballismus

29
Q

hemiballismus due to lesion where?

A

contralateral subthalamic nuc (usually via ischemic infarct)

30
Q

continual sustained contraction of muscle leading to spasm (often painful)

A

dystonia

31
Q

stereotyped repetitive focal muscle contractions that appear semipurposeful

A

tics

32
Q

Tourette’s- gender and accompanying conditions

A

seen in boys

behavioral disorders/ADHD

33
Q

rapid shock-like lightning movements/jerks of limbs and trunk - typically bilateral

A

myoclonus

34
Q

myoclonus can be seen in which dz

A

Creutzfeldt-Jakob

35
Q

semi-rhythmic loss of postural control of hands and feet - tremor seen when extended - “flapping”

A

asterixis

36
Q

tx for resting tremor

A

anticholinergics or levodopa and DA agonists

37
Q

tx for essential tremor

A

beta blockers or barbituates

38
Q

tx for choreoathetosis

A

DA antagonist

39
Q

tx for hemiballismus

A

DA antagonist

40
Q

tx for tics

A

DA antagonist

41
Q

tx for dystonia

A

anticholinergics, benzos, botulinum toxin injections