Chapter 8: Ataxia and Gait Disorders Flashcards

1
Q

Which part of neuraxis causes ataxia

A

Cerebellar or sensory ataxia

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2
Q

Vermis vs. Hemispheric Cerebellar lesions

A

Vermal lesions: truncal and gait ataxia

Hemispheric lesions: Ipsilateral limb ataxia

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3
Q

Cerebellar Hemorrhage/Infarction

A

Abrupt onset of vertigo, vomiting, and inability to walk.
Level of arousal may be depressed if their is compression of fourth ventricle with hydrocephalus
Need neurosurgical decompression

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4
Q

Alcoholic Cerebellar Degeneration

A

Damages the vermis (truncal and gait ataxia)
Most common cause of acquired cerebellar degeneration.
Accompanied commonly by alcoholic polyneuropathy

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5
Q

Postinfectious Cerebellitis

A

Children age 2-7
Follows VZV or other virus
Limb, gait ataxia and dysarthria
Complete recovery

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6
Q

Paraneoplastic Cerebellar Degeneration

A

Pancerebellar syndrome: Truncal, gait, and limb ataxia; dysarthria; ocular motility issues (ocular dysmetria, nystagmus)
Acute/Subacute and then stabilizes with profound disability
Associated with Gynecologic or small cell lung cancer
CSF: elevated protein or lymphocytic pleocytosis
Anti-Yo, anti-Hu antibodies

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7
Q

Friedreich Ataxia

A

Aut. rec.
Progressive ataxia arms>legs, severe dysarthria
Childhood onset
Loss of reflexes, spasticity and extensor plantar responses, impaired vibration and position sense

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8
Q

Intention tremor

A

Rhythmic side-to-side oscillations of the limb as it approaches the target

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9
Q

Dysdiadochokinesia

A

Abnormality of rapid alternating movement (RAM)

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10
Q

Gait ataxia

A

Broad-based and unsteady

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11
Q

Dysarthria

A

Slow scanning and monotonous speech

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12
Q

Scanning speech

A

Pausing in between syllables of words, putting unusual emphasis or force on syllables

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13
Q

Drugs that cause ataxia

A

Phenytoin, barbiturates, antineoplastic agets

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14
Q

Inherited Episodic Ataxia

A

Brief episodes of ataxia, vertigo, nausea, and vomiting

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15
Q

Autosomal Dominant Spinocerebellar Degenerations

A

Cerebellar ataxia with or without additional neurologic signs.
Insidious onset

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16
Q

Miller Fisher Syndrome

A

Triad of ataxia, areflexia, and ophthalmoplegia.
Due to proprioceptive loss rather than to cerebellar dysfunction.
Variant of Guillain Barre, due to a postinfectious immune process most likely.
IgG anti-GQ1b
Good prognosis

17
Q

Cerebellar Stroke

A

Sudden onset of cerebellar ataxia, vomiting, depressed consciousness

18
Q

Common cause of ataxia in children

A

Postinfectious cerebellitis

19
Q

Small cell lung cancer or gynecologic malignancy and ataxia

A

Paraneoplastic cerebellar degeneration

20
Q

Hemiparetic gait

A

Stiff leg and toes scrape the floor

21
Q

Paraparetic

A

Bilateral hemiparesis, adductor tone increased and legs cross with walking (scissoring gait)

22
Q

Akinetic-Rigid Gait

A

Parkinsonian gait. Shuffling, slow with short steps and reduced arm swing.
Progressive supranuclear palsy is that the posture tends toward extension rather than flexion.
Basal ganglia

23
Q

Frontal Gait

A

Flexed posture
Small, shuffling, and hesitant steps
Magnetic: difficulty lifting feet off the ground

Hydrocephalus, tumor, stroke, neurodegeneration

24
Q

Waddling gait

A

hip-girdle weakness, abductor muscle weakness (glutes)
Trendelenberg gait

Muscular dystrophy, spinal muscular atrophy, acquired proximal myopathy

25
Q

Sensory ataxia

A

Slapping gait
Loss of proprioceptive input from the feet
Cautious, wide based, slow steps

Large-fiber neuropathy: B12 deficiency
Dorsal columns: Tabes dorsalis

26
Q

Psychogenic gait

A

There is good strength and postural reflexes, so they lurch without falling

27
Q

Hemiparetic gait

A

Hemispheric dysfunction, most likely from a stroke

28
Q

Paraparetic gait

A

Spinal cord disease
Multiple sclerosis, transverse myelitis, compressive myelopathy.

May be diffuse anoxic injury to the brain

29
Q

Hydrocephalus (including NPH), neurodegenerative process, or bifrontal or diffuse subcortical disease

A

Frontal gait

30
Q

Ophthalmoplegia

A

Also known as ophthalmoparesis

Weakness/paralysis of one or more extraocular muscles