Neurology Flashcards

1
Q

Imaging in stroke?

A

Non-contrast CT head

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2
Q

First line drug in myoclonic seizures (women)?

A

Leviteracitam

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3
Q

What is a Jacksonian movement and the it is observed?

A

Clonic movement travelling proximally
Frontal lobe epilepsy

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3
Q

Level at the spinal cord is affected in autonomic dysreflexia?

A

Above T6

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4
Q

Areas affected in the brain in Alzheimer’s disease?

A

Widespread cerebral atrophy
Cortex and hippocampus

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5
Q

Movements spared in MND?

A

Occular movement

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6
Q

Which intracranial bleed can present several weeks after injury?

A

Subdural haematomas

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7
Q

When should LP be performed in SAH?

A

12 hours post onset of headache

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8
Q

Dermatome of sciatic nerve?

A

S1

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9
Q

UMN tests?

A

UL: Hofman’s
LL: Babinski’s

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10
Q

Signs of idiopathic intracranial hypertension?

A

Papilloedema
6th nerve palsy

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11
Q

If suspected TIA and patient is on warfarin/DOAC?

A

ED for imaging to exclude haemorrhage

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12
Q

Horner’s syndrome?

A

Ptosis and constricted pupil

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13
Q

CN3 findings?

A

Down and out
Dilated pupil

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14
Q

Weber’s syndrome?

A

Crossed findings due to brain stem infarcts
Ipsilateral CN3 palsy
Contralateral hemiplegia or hemiparesis

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15
Q

Symptoms in subacute degeneration of the cord?

A
  1. Loss of proprioception and vibration sense (dorsal columns)
  2. Spasticity and brisk reflexes (lateral columns)
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16
Q

Risk factor for pontine haemorrhage?

A

Chronic HTN

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17
Q

Pontine haemorrhage symptoms and signs?

A

Reduced GCS
Quadraplegia
Miosis
Absent horizontal eye movement

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18
Q

Symptoms in neurogenic thoracic outlet syndrome?

A

Muscle wasting in hands
Numbness and tingling
Autonomic symptoms

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19
Q

Symptoms of autonomic dysreflexia?

A

Severe HTN
Sweating above level of the lesion
Agitation

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20
Q

Complication of autonomic dysreflexia?

A

Haemorrhagic stroke

21
Q

After clinical diagnosis of spinal stenosis what is the next step?

A

MRI to confirm diagnosis and exclude other pathology

22
Q

Lateral medullary syndrome (Wallenberg’s syndrome) symptoms?

A

Ipsilateral: Ataxia, nystagmus, dysphagia, facial numbness, CN palsy
Contralateral: Limb sensory loss

23
Q

MND with worse prognosis?

A

Progressive bulbular palsy

24
Most common earliest symptom in spinal cord compression?
Back pain
25
What is angiomyolipoma associated with?
Tuberous sclerosis
26
First line management in atonic or tonic seizure in females?
Lamotragine
27
Which nerve does finger abduction?
Ulnar
28
Which nerve does finger extension?
Radial
29
Parsonage-Turner's syndrome?
Peripheral neuropathy, complication of viral illness, resolves spontaneously
30
Type of scan required to view demyelinating lesions (as in MS)?
Contrast MRI
31
Gold standard test for venous sinus thrombosis?
MR venogram
32
Barthel index?
Scale that measures disability or dependence in activities of daily living in stroke patients
33
Lesions at T1?
Cause finger abduction weakness
34
Acute ischaemic stroke CT sign?
'hyperdense artery' sign (usually visible immediately in contrast to changes in the parenchyma)
35
Management of SAH?
Coiling of aneurysm
36
Isolated seizure and normal EEG affect on driving?
Patients cannot drive for 6 months following a first unprovoked or isolated seizure if brain imaging and EEG normal
37
What artery supplies Broca's area?
Middle cerebral artery (on dominant side of brain)
38
Relapsing remitting MS?
Acute attacks followed by periods of remission (85%)
39
Secondary progressive MS?
Relapsing and remitting has deteriorated and patient has developed neuro signs and symptoms between relapses
40
Primary progressive MS?
Progressive deterioration from onset (10%, more common if older)
41
management if dent on head after injury?
Immediate CT ?depressed skull fracture
42
When is thrombectomy indicated in stoke?
6-24 hour window if potential to salvage brain tissue (limited infarct core volume)
43
Presentation of syringomyelia?
Cape-like loss of pain and temperature sensation duets compression of spinothalamic tract fibres Strong association with Chari malformation
44
Acute intermittent porphyria presentation?
Abdominal, neurological and psych symptoms
45
Management of acute porphyria?
IV haem arginate / haematin If not available give IV glucose
46
Electrolyte abnormality in SAH?
Hyponatrameia
47
Uhtoff’s phenomenon?
Neuro signs worse with increase in body temp (E.g worse vision when running)
48
Brown- sequadrad syndrome?
Spinal cord hemisection Ipsilateral spastic paresis below lesion Ipsilateral loss of proprioception and vibration sense Contra lateral loss of pain and temp
49
Which PD drugs are associated with the highest chance of inhibition disorders out of the antiparkinsonian medications?
Dopamine receptor agonists