Examination - Neurological Flashcards

(35 cards)

1
Q

What is the main differential of an abnormal gait with a flexed arm?

A

Hemiplegia

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2
Q

What are the 4 cardinal features of upper motor neurone hemiplegia?

A
  • increased tone
  • > 5 beats of clonus
  • hypereflexia
  • +ve Babinski reflex
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3
Q

What type of gait is seen in hemiplegia with a flexed arm and extended leg?

A

Circumductive

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4
Q

What signs indicate bulbar involvement of stroke?

A

CN9, 10, 11, 12
pseudobulbar - UMN - increased gag reflex and jaw jerk
bulbar - LMN - reduced gag reflex and jaw jerk

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5
Q

How is power graded?

A
0 = none 
1 = flicker 
2 = moves with gravity 
3 = moves against gravity
4 = reduced power against resistance
5 = normal
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6
Q

How are strokes classified?

A

Bamford classification

  • Total anterior circ stroke = hemiplegia, homonymous hemianopia, higher cortical dysfunction (unlikely to have in OSCE)
  • Partial anterior circ stroke = 2 of the 3
  • Lacunar circ stroke = hemimotor or hemisensory stroke only
  • Posterior circ stroke
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7
Q

What is the main differential for an abnormal slow shuffling gait?

A

Parkinsonism

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8
Q

What are some of the signs of parkinsonism?

A
Bradykinesia
Rigidity
Shuffling gait 
Resting tremor pill-rolling
Cogwheel rigidity
Glabellar tap +ve (Parkinsons patients will blink repeatedly) - always ask permission 
Reduced arm swing

Features are usually worse on one side

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9
Q

Why would you want to measure the lying and standing BP in a patient with parkinsonism?

A

To rule out multisystem atropy

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10
Q

Why would you want to assess the eye movements in a patient with parkinsonism?

A

to rule out progressive supranuclear palsy

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11
Q

Why would you want to assess higher cognitive function in a patient with parkinsonism?

A

to rule out Lewy-Body dementia or Parkinsons dementia

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12
Q

What are the causes of parkinsonism?

A
  • Idiopathic Parkinsons disease
  • Multisystem atrophy - postural hypotension
  • Progressive supranuclear palsy - palsy of vertical eye movements
  • Lew-body dementia - dementia onset <12 months after parkinsonism
  • Corticobasal degeneration - apraxia, acalculia, myoclonus
  • Drug-induced - Hx of antipsychotics
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13
Q

How is Parkinsons disease treated?

A

Symptom control (do not alter disease progression)

  • L-dopa
  • Co-beneldopa -
  • Pergolide
  • Apomorphine
  • Selegiline
  • Entacapone
  • Procyclidine
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14
Q

What is the main differential of an abnormal gait that is broad and unsteady with poor heel to toe balance?

A

Cerebellar syndrome

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15
Q

What are the features of cerebellar syndrome?

A
DANISH 
Dysdiadokinesis
Ataxia
Nystagmus
Intention tremor
Slurred speech
Hypotonia
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16
Q

Where is the cerebellar lesion localised when there is truncal ataxia with minimal limb signs?

A

Cerebellar vermis

17
Q

Where is the cerebellar lesion localised when there is ipsilateral limb signs with less truncal involvement?

A

Cerebellar hemisphere

18
Q

What is the most likely cause of the cerebellar syndrome if the patient is younger, female with spasticity and internuclear opthalmoplegia?

A

Multiple sclerosis

19
Q

What is the most likely cause of the cerebellar syndrome if the patient is older with atrial fibrillation, CABG scarring and tar staining?

20
Q

What is the most likely cause of the cerebellar syndrome if the patient has a comorbidity of chronic liver disease?

21
Q

What is the most likely cause of the cerebellar syndrome if the has coarse facial features and gingivial hypertrophy?

A

Phenytoin use

22
Q

Where is the lesion that causes internuclear opthalmoplagia?

A

Medial longitudinal fasciculus - failure of conjugate gase so eyes do not move in synchrony

23
Q

How does internuclear opthalmoplegia present on examination?

A

Ipsilateral failure of adduction and contralateral nystagmus when in abduction

24
Q

How is multiple sclerosis treated?

A

Methylprednisolone to shorten the duration of acute attacks.
Baclofen for muscle spasm.
Disease modifiers [reduce the frequency and duration of flare-ups]: interferone-beta, galtriamer, alemtuzumab

25
What are the two differentials of facial weakness?
Lower CN7 palsy - ipsilateral | Upper CN7 palsy - contralateral and forehead sparing
26
What is the likely diagnosis in CN 5, 6 and 8 palsy?
Acoustic neuroma
27
What is the likely diagnosis in isolated CN8 palsy?
Cholesteatoma - inner ear affected
28
What is the likely diagnosis in facial palsy with parotid swelling/scar?
Parotid tumour
29
What is the likely diagnosis in a facial palsy associated with a vesicular rash on the ear?
Ramsay-Hunt Syndrome
30
What are the secondary causes of facial nerve palsy?
- Stroke - MS - Myaesthenia gravis - Ramsay-Hunt syndrome - Lyme disease - Diabetes mononeuropathy - Tumour - Gullarin-Barre sydrome - Sarcoidosis
31
What is the likely diagnosis in bilateral facial palsy with bullseye-lesions on the skin?
Lyme disease
32
What is the treatment of Bell's palsy?
eye protection & prednisolone
33
What is the most likely diagnosis for weakness with fasciculations, increased tone, mixed UMN and LMN signs, upgoing plantars, bulbar involvement and a normal sensory examination?
Motor neurone disease
34
What are the differential diagnoses for mixed UMN and LMN signs?
- MND - Dual pathology e.g. peripheral neuropathy + stroke - Conus medullaris lesion - L1 lesion - B12 deficiency - subacute combined degeneration of the cord
35
Does multiple sclerosis have UMN or LMN signs?
UMN ONLY