Neuro Flashcards

1
Q

What does left homonymous hemianopia mean?

A

Visual field defect to the left

Ie right optic tract lesion

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2
Q

A 42-year-old woman is admitted to the vascular ward for an endarterectomy. Her CT report confirms a left temporal lobe infarct.
Visual field defect?

A

Right superior quadranopia

Temporal lesions cause a contralateral superior quadranopia. Think temporal area is at the top of the head i.e. superior quadranopia

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3
Q

A 22-year-old man is referred to urology with possible urinary retention. He is passing huge amounts of urine. Post void bladder ultrasound is normal.
Visual field defect?

A

Lower bitemporal hemianopia

This patient has diabetes insipidus due to a craniopharyngioma. This causes a lower bitemporal hemianopia.

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4
Q

A 53-year-old man is admitted to the vascular ward for a carotid endarterectomy. His CT head report confirms a left parietal lobe infarct.
Visual field defect?

A

Right inferior quadranopia

Parietal lesions cause a contralateral inferior quadranopia.

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5
Q

How to remember homonymous quadranopias ?

A

PITS
Parietal Inferior
Temporal Superior

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6
Q

What is visual field defect when a pit adenoma compresses?

A

Bitemporal hemaniopia

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7
Q

With a bitemporal hemaniopia
If the defect is mostly Upper quadrant where is the compression?
Lower quadrant?

A

Upper - from inferior side
-Eg Pituitary adenoma

Lower - from superior
-Eg Craniopharyngioma

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8
Q

What condition do you see bilateral acoustic neuromas ? Ix?

A

Neurofribromatosis type 2

MRI of cerebellopontine angle

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9
Q

To stop antiepileptics

How long seizure free? How long do you spend stopping drugs?

A

Can be considered if seizure free for > 2 years, with AEDs being stopped over 2-3 months

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10
Q

Why do you not use carbamazepine in absence seizures?

A

Can exacerbate them

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11
Q

What happens in Wallenberg s?

A

Lateral medullary syndrome (posterior inferior cerebellar artery)

ipsilateral: ataxia, nystagmus, dysphagia, facial numbness, cranial nerve palsy e.g. Horner’s
contralateral: limb sensory loss

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12
Q

Vessel with Contralateral hemiparesis and sensory loss, lower extremity > upper

A

Anterior cerebral

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13
Q

Vessel with Contralateral hemiparesis and sensory loss, upper extremity > lower
Contralateral homonymous hemianopia
Aphasia

A

Middle cerebral

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14
Q

Contralateral homonymous hemianopia with macular sparing
Visual agnosia
Vessel?

A

Posterior cerebral artery

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15
Q

Vessel? Ipsilateral CN III palsy

Contralateral weakness of upper and lower extremity

A

Weber syndrome

Posterior cerebral

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16
Q

Ipsilateral: facial pain and temperature loss
Contralateral: limb/torso pain and temperature loss
Ataxia, nystagmus
Vessel?

A

Posterior inferior cerebellar

Wallenberg syndrome

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17
Q

What is complex regional pain syndrome?

A

Often after minor injury

  • > disproportionate Sx to original injury
  • temperature and skin changes
  • oedema and sweating
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18
Q

What needs to be considered before starting IV phenytoin? Why?

A

Cardiac monitoring

-proarrhythmogenic effects

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19
Q

When would you check phenytoin levels?

A

Before dose if:
1- adjustment in dose
2- suspected toxicity
3- suspected non adherence

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20
Q

Which drugs can -> myasthenia crisis?

A
penicillamine
quinidine, procainamide
beta-blockers
lithium
phenytoin
antibiotics: gentamicin, macrolides, quinolones, tetracyclines
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21
Q

Usual cause of a painful CNIII palsy?

A

Posterior communicating artery aneurysm

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22
Q

Features of CNIII palsy?

A

Eye deviated down and out
Ptosis
Pupil may be dilated

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23
Q

What is Lennox-gastaut syndrome thought to perhaps follow? Usual age?
Seen on EEG? What may help?

A
May be extension of infantile spasms (50% have hx)
onset 1-5 yrs
atypical absences, falls, jerks
90% moderate-severe mental handicap
EEG: slow spike
ketogenic diet may help
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24
Q

Sodium valproate mechanism? Adverse effects?

A

Increases GABA

Appetite and weight gain 
P450 enzyme inhibitor (Eg think warfarin) 
Ataxia 
Tremor 
Hepatitis 
Pancreatitis 
Thrombocytopenia 
Alopecia 
Teratogenic - neural tube
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25
Q

Carbamazepine mechanism? Adverse effects

A

Binds to Na channels -> increases refractory period

P450 enzyme inducer 
Dizzy / ataxia 
Drowsiness 
Lecupenia and agranulocytosis 
SIADH 
Visual disturbances
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26
Q

Lamotrigine mechanism? Adverse effects ?

A

Na channel blocker

Stephen Johnson’s

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27
Q

Phenytoin mechanism? Adverse effects ?

A

Binds to Na channel -> increase refractory period

P450 inducer 
Dizzy and ataxia 
Drowsiness 
Gingival hyperplasia, hirtuism, coarsening of facial features 
Megaloblastic anaemia 
Peripheral neuropathy 
Increased vit d metabolism -> osteomalacia 
Lymphadenopathy
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28
Q

Which drug increased life span in MND

A

Riluzole

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29
Q

Key distinguishing features of Lewy body dementia

A

Progressive cognitive impairment
Parkinsonism
Visual hallucinations

SPECT scan can be used

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30
Q

First seizure and DVLA?

A

Inform
6 months off driving so long as no structural abnormalities and no eleptiform activity on EEG

If either of these -> 12 months seizure free

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31
Q

Following stopping epilepsy medication how long should people not drive

A

6 months after last dose

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32
Q

1st line anti thrombotic post TIA/stroke ?

A

Clopidogrel

Aspirin + dipyridamole for those who cannot tolerate

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33
Q

What are the features of syringomyelia ?

Strong association?

A

Slow progressing

Motor- Wasting and weakness of arms
Sensory - Spinothalamic sensory loss (pain and temp)
Loss of reflexes

Arnold-chiari malformation

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34
Q

Key feautres of guillian barre

A

Often post gastroenteritis

Ascending weakness
Areflexia
Autonomic - eg urinary retention
Cranial nerve involvement

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35
Q

MG associations

A

Thymic hyperplasia / thyromas

Autoimmune - Pernicious anaemia, autoimmune thyroid, SLE, Rhematoid arthritis

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36
Q

5 Ix in MG?

A
Nerve conduction studies 
CT thorax - exclude thyroma 
Creatine kinase - Normal 
Autoantibodies 
Tension test
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37
Q

3 key long term Mx of MG

A

Long acting anti-cholinesterase - Eg pyridostigmine
Immunosuppression - prednisolone
Thymectomy

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38
Q

Mx of MG crisis?

A

Plasmapheresis

IVIG

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39
Q

TS inheritance?

A

Autosomal D

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40
Q

Cutaneous / neurological features in TS?

A

Cutaneous
Ash leaf spots which fluoresce under UV light
Rough patches of skin over lumbar spine (shagreen patches)
Angiofibromas in butterfly distribution over nose
Fibromata under nails

Neurological
Developmental delay
Epilepsy
Intellectual impairment

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41
Q

Features of multi system atrophy

A

Parkinsonism
Autonomic - Atonic bladder, postural hypotension
Cerebellar signs

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42
Q

What happens in b12 deficiency

A

Subacute combined degeneration of the spinal cord

  • dorsal colum usually affected first (Proprioception, vibration)
  • > distal parathesia
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43
Q

Status epliepticus

1/2/3rd line Mx?

A

1 Buccal midazolam/ IV lorazepam
2 IV lorazepam
3 IV phenytoin (phenobarbital if already on regular phenytoin)
4 Rapid sequence induction of anaesthesia using thiopental sodium

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44
Q

Cranial nerves affected in acoustic neuroma

A

cranial nerve VIII: hearing loss, vertigo, tinnitus

cranial nerve V: absent corneal reflex

cranial nerve VII: facial palsy

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45
Q
Common reflex roots
Ankle?
Knee?
Biceps?
Triceps?
A

Ankle S1-S2
Knee L3-L4
Biceps C5-C6
Triceps C7-C8

46
Q

Which anti-epileptic most associated with weight gain?

47
Q

Mid humeral fracture
Which nerve are you worried about?
How to test?

A

Radial

Extend the wrist

48
Q

Migrane during pregnancy 1st and 2nd line

A

1 - paracetamol 1g

2- ibuprofen / aspirin if in 1st/2nd trimester

49
Q
What class of drug used in Mx of chemo related nausea ? EG?
Where do they act? Common Side effect?
A

5-HT3 antagonists
Odansetron

Medulla oblongata

Constipation

50
Q

What can provoke an absence seizure? Seen on EEG?

A

Hyperventilation / stress

Bilateral symmetrical 3Hz spike and wave

51
Q

Management of cervical myelopathy due to disk prolapse

A

Cervical decopressive surgery

-> ideally within 6 months of diagnosis for bet prognosis

52
Q

Ix if cervical myelopathy is suspected?

A

MRI of spine

53
Q

What is cataplexy? Association?

A

Sudden transient loss of muscular tone caused by strong emotion

2/3 of narcolepsy patients have cataplexy

54
Q

What would you expect in raising eyebrow in Bell’s palsy

A

Inability to do so as it is a LMN palsy of facial nerve

55
Q

Mx of Bell’s palsy

A

Prednisolone

Eye care - eg artificial tears

56
Q

What Class of drug do you really need to avoid in LB dementia

A

Antipsychotics -> they are v sensitive and can lead to irreversible Parkinsonism

57
Q

What is hereditary sensorimotor neuropathy also called?
Inheritance?
Features? Usual presentation?

A

Charcot-Marie-tooth disease
AD

Starts at puberty
Motor sx predominate
-Distal muscle wasting, clawed toes
-Foot drop, leg weakness are the usual presenting features

58
Q

Eg of dopamine receptor antagonist for Parkinson’s? Big adverse effect? Other S/e?

A

Bromocriptine, ropinirole, carbegoline

Pulmonary / cardiac fibrosis

Impulse control disorders, daytime somnolence, hallucinations

59
Q

What is often used to treat drug induced Parkinsonism? Eg?>

A

Anti muscarinic

Procyclidine, benzotropine

60
Q

Which commonly used anaesthetic agent are people with MG resistant to?

A

Suxamethonium

61
Q

Restless leg syndrome
What is it? Features? Associations?
Diagnosis? Mx?

A

Uncontrollable urge to move legs (akathisa)

  • usually at night
  • Can get parathesia / throbbing
  • May occur during sleep
FHx
Iron deficiency anaemia 
Uraemia
Diabetes 
Pregnancy 

Diagnosis is clinical although bloods to exclude Iron deficiency anaemia

Mx
Walking, stretching / massaging affected limbs
Treat iron deficiency
Dopamine agonists (Pramipexole / ropinirole)
Benzos
Gabapentin

62
Q

Where is the defect ?

A 72-year-old man develops visual problems. He is noted to have a left homonymous hemianopia with some macula sparing.

A

Occipital cortex

[macular sparing]

63
Q

Where is the defect?
A 30-year-old man with a family history of early blindness is concerned that he is developing ‘tunnel vision’.
What else could be seen on exam ?

A

Retina
This is probably retinitis pigmentosa

Extensive pigmentation seen on fundoscopy

64
Q

What is miosis

A

Contracted pupil

65
Q

Seen in CNIII palsy?

A

Eye down and out
Ptosis
Pupil may be dilated

66
Q

Tremor worse when arms outstretched
Improved by alcohol and rest
Strong FHx

A

Essential tremor

67
Q

Tremor with history of liver disease

A

Hepatic encephalopathy

68
Q

Tremor with COPD hx

A

Carbon dioxide retention

69
Q

Parkinsonism with Supra nuclear palsy has what distinguishing features ?

A

Dysarthria

Reduced verticals eye movements

70
Q

Which drug used fro stroke thrombolysis ?

71
Q

Mx of ischemic stroke after 4.5hour window missed?

72
Q

When do people develop a high stepping gait? What would you suspect if unilateral?

A

Peripheral neuropathy

Common peroneal nerve lesion

73
Q

Loss of corneal reflex

A

Think acoustic neuroma

74
Q

Nerve to deltoid

75
Q

Feaures of Bell’s palsy

A

Paralysis Forehead affected - LMN

Dry eyes, altered taste

76
Q

Mx of Bell’s palsy

A

Prednisolone 10 days

Artificial tears

77
Q

An 8-year-old boy falls onto an outstretched hand and sustains a supracondylar fracture. In addition to a weak radial pulse the child is noted to have loss of pronation of the affected hand.
Nerve?

78
Q

LMN/UMN in ALS, PLS, PMA

A

myotrophic lateral sclerosis (50% of patients)
typically LMN signs in arms and UMN signs in legs
in familial cases the gene responsible lies on chromosome 21 and codes for superoxide dismutase

Primary lateral sclerosis
UMN signs only

Progressive muscular atrophy
LMN signs only
affects distal muscles before proximal
carries best prognosis

Progressive bulbar palsy
palsy of the tongue, muscles of chewing/swallowing and facial muscles due to loss of function of brainstem motor nuclei
carries worst prognosis

79
Q

Post shingles pain doesn’t respond to paracetamol and ibuprofen . Give what?

A

Amitriptyline

80
Q
Essential tremor 
Better or worse with 
Alcohol?
Hand outstretched ?
1st line?
A

Better with alcohol worse outstretched

Propranolol

81
Q

Features of subacute degeneration of the spinal cord

A
  1. Bilateral spastic paresis
  2. Bilateral loss of proprioception and vibration sensation
  3. Bilateral limb ataxia
82
Q

Syngomyella features

A
  1. Flacid paresis (typically affecting the intrinsic hand muscles)
  2. Loss of pain and temperature sensation
83
Q

Neurosyphylis sensation features?

A

Loss of proioception and vibration

84
Q

A 32-year-old rugby player is hit hard on the shoulder during a rough tackle. Clinically his arm is hanging loose on the side. It is pronated and medially rotated.

A

Brachial trunks c5-6

-Erbs palsy

85
Q

A 42-year-old teacher is admitted with a fall. An x-ray confirms a fracture of the surgical neck of the humerus. Which nerve is at risk?

86
Q

A 63-year-old man is admitted with a severe headache, nausea and a recent epileptic fit. Fundoscopy shows papilloedema. He is also noted to have diplopia when asked to look laterally.
Nerve?

87
Q

A 32-year-old lady is admitted with weakness, visual disturbance and periorbital pain. On examination she is noted to have mydriasis and diminished direct response to light shone into the affected eye. The consensual response in the affected eye is preserved.
Nerve?

88
Q

A 60 year-old male presents with clumsy hands. He has been dropping cups around the house. His wife complains he doesnt answer his mobile as he struggles to use it. His symptoms have been gradually deteriorating over the preceding months.
Sign ?

A

Hoffmans

[This patient is likely to have degenerative cervical myelopathy [DCM], which is associated with upper motor neuron signs. Hoffmans sign is elicited by flicking the distal phalaynx of the middle finger to cause momentary flexion. A positive result is exaggerated flexion of the terminal phalanyx of the thumb. Patients with DCM often have subtle signs that are easily missed [1], but as a progressive condition, these are likely to get worse [2]. Whilst the sensitivity of signs is low (i.e. their absence does not rule out a problem), their specificity is high (i.e. there will be a problem). Therefore, in order to diagnose early DCM and improve patient outcomes, a high index of suspicion, alongside a comprehensive neurological examination and monitoring for progression is required.]

89
Q

A 32 year-old female presents with a 3 day history of altered sensation of her left foot and right forearm. She had an episode of visual loss a few months ago and says her friends have noted her eyes be flickery and jerky.
Sign?

A

Hoffmans

[This patient is likely to have Multiple Sclerosis (MS). As a disease of the central nervous system, MS is usually associated with only upper motor neuron signs such as Hoffmans sign (see above). The patients visual loss was probably secondary to optic neuritis, a common presentation of MS. Cerebellar signs are particularly common with MS and include nystagmus, which is likely to be the jerky eye movements noted by her friends.]

90
Q

A 70 year old man has decompressive surgery for degenerative cervical myelopathy. Three years later he presents with neck pain and hand paraesthesias. Which one of the following management strategies is recommended?

A

Urgent referral -

[Postoperatively, patients with cervical myelopathy require ongoing follow-up as pathology can ‘recur’ at adjacent spinal levels, which were not treated by the initial decompressive surgery.

Recurrent symptoms should be treated with a high degree of suspicion. Although peripheral neuropathy can occur in any patient, this should not be the diagnosis that is the most strongly suspected as delays in diagnosis and treatment of DCM affect outcomes. ]

91
Q

Common side effect of Triptans

A

‘triptan sensations’ - tingling, heat, tightness (e.g. throat and chest), heaviness, pressure

92
Q

Triptans CI

A

patients with a history of, or significant risk factors for, ischaemic heart disease or cerebrovascular disease

93
Q

Drug to reduce tremor in drug induced Parkinsonism

A

Procyclidine

94
Q

Why don’t you get sensory loss over the distribution of the facial nerve in Bell’s palsy?

A

The facial nerve does not carry sensation

95
Q

Why do you get hyperacusis in Bell’s palsy ?

A

Paralysis of stapedius

96
Q

Facial nerve supplies?

A

Supply - ‘face, ear, taste, tear’

face: muscles of facial expression
ear: nerve to stapedius
taste: supplies anterior two-thirds of tongue
tear: parasympathetic fibres to lacrimal glands, also salivary glands

97
Q

IIH associated medications?

A
contraceptives
steroids
levothyroxine
lithium
Tetracycline Abx
98
Q

What condition do you see bilateral acoustic neuromas ?

A

Neurofibromatosis type 2

99
Q

Ix in acoustic neuroma

A

MRI of cerebellopontine angle

100
Q

You are examining a patient who complains of double vision. Whilst looking forward the patient’s right eye turns upwards and outwards. On attempting to look to the patient’s left the right eye elevates more as it moves medially. On looking right there is no obvious squint. What is the most likely underlying problem?

A

Right 4th nerve palsy

Supplies superior oblique

101
Q

What is Webber syndrome

A

Pattern of stroke

  • ipsilateral III palsy
  • contralateral weakness
102
Q

Useful in patients with absence seizures who are intolerant of sodium valproate

A

Ethosuximide

103
Q

Mechanism of odansetron? Common side effect?

A

5-HT3 antagonist

Constipation

104
Q

A 40-year-old man presents with a progressive deterioration in vision over the past 2 weeks. On examination, there is ophthalmoplegia, his gait is noticeably ataxic and there is a generalised loss of the deep tendon reflexes. He returned from Turkey two weeks ago where he describes having a simple viral illness involving a sore throat and fever that lasted for around 1 week and resolved shortly before his return home. He drank more alcohol than normal during the holiday, having around 3 glasses of wine each night. What is the cause of his poor vision?

A

Miller-Fisher variant
§ is a type of Guillain-Barre syndrome that starts by affecting the cranial nerves and therefore manifests with eye signs. Both Guillain-Barre syndrome and Miller-Fisher tend to be preceded by an infection, classically Campylobacter jejuni.

Ophthalmoplegia, areflexia and ataxia (of which the question has all three) are the major features of Miller-Fisher.

This alcohol consumption is a distractor as the question states he drank much more than usual this week and alcoholic polyneuropathy only comes from a chronic, heavy alcohol history.

105
Q

Open angle glaucoma visual loss?

A

Peripheral vision loss in affected eye

106
Q

What is gastroschisis ? Exomphalos? Associations?

A

Gastroschisis describes a congenital defect in the anterior abdominal wall just lateral to the umbilical cord
-Gastroschisis is associated with socioeconomic deprivation (maternal age <20, maternal alcohol/tobacco use)

In exomphalos the abdominal contents protrude through the anterior abdominal wall but are covered in an amniotic sac formed by amniotic membrane and peritoneum

107
Q

What is Epstein’s pearl? Mx?

A

A congenital cyst found in the mouth. They are common on the hard palate, but may also be seen on the gums where the parents may mistake it for an erupting tooth.

No treatment is generally required as they tend to spontaneously resolve over the course of a few weeks.

108
Q

When is mirtazapine particularly useful? Class?

A

specific serotonergic antidepressant
Increases appetite and sedative
[old people with insomnia and poor appetite]

109
Q

Brocca vs wernickes

A

Wernickes - receptive dysphasia -
-fluent speech, but abnormal comprehension

Brocca - Expressive dysphasia
-Poor speech but normal comprehension

110
Q

Sx of SSRI discontinuation?

A

Dizziness, electric shock sensations and anxiety

111
Q

Cerebellar vermis vs hemisphere ataxia?

A

Cerebellar hemisphere lesions cause peripheral (‘finger-nose ataxia’)

Cerebellar vermis lesions cause gait ataxia