Neuro PTS Flashcards

1
Q

Symptoms facial nerve palsy

A

Facial weakness
Altered taste (anterior 2/3 tongue)
Unable to close eyes
Hyperacusis (sensitivity to sound)

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2
Q

Distinguishing feature of UMN lesion vs LMN lesion in a facial nerve palsy

A

UMN: frontalis and orbicularis oculi muscles preserved (forehead sparing) - lesion A
LMN: forehead muscles NOT preserved - lesion B

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3
Q

Causes of LMN facial nerve palsy + treatment for each (2)

A

Bell’s palsy - steroids
Ramsay Hunt (herpes zoster) - acyclovir

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4
Q

Clinical presentation of trigeminal neuralgia

A

Stabbing pains
Unilateral
Usually 1 distribution
No symptoms between attacks

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5
Q

Examples of pain relief in trigeminal neuralgia

A

Carbamazepine
Gabapentin/lamotrigine/phenytoin

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6
Q

Median nerve muscle innervation (4)

A

LOAF

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7
Q

Median nerve origination

A

C5 - T1

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8
Q

Median nerve sensory innervation

A
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9
Q

2 treatments for a median nerve lesion

A

Splinting
Corticosteroid injection

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10
Q

Peripheral nerve revision

A

Ulnar nerve
Radial nerve
Lateral cutaneous nerve of the thigh
nerves of the foot

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11
Q

Symptoms of UMN lesion

A

Everything goes UP
Hyperreflexia
Hypertonia
Up going plantars
Spasticity

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12
Q

Symptoms of LMN lesion

A

Hyporeflexia
Hypotonia

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13
Q

Types of MND

A

Amyotrophic lateral sclerosis - most common
Progressive bulbar palsy - second most common (primarily affects talking + swallowing)
Progressive muscular atrophy
Primary lateral sclerosis

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14
Q

ALS pathophysiology

A

Progressive degeneration of both upper and lower motor neurones - sensory neurones are spared

Genetic component 5-10% cases (family history important)

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15
Q

Typical ALS patient presentation

A

Late middle aged man possibly with an affected relative
Insidious progressive weakness of the muscles throughout the body affected the limbs, trunk, face and speech (often first noticed in the upper limbs)
Clumsiness,
Dysarthria (slurred speech)

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16
Q

Investigation for motor neurone disease

A

Electromyography - fasciculations and fibrillations

17
Q

Diagnosis MND

A

Clinical presentation and exclusion of other conditions

18
Q

Management MND

A

Riluzole (extends life)
Baclofen for symptom control
Non-invasive ventilation

Prognosis: fatal, 3-5 years

19
Q

Types of seizure (need to redo all of this)

A

Tonic - generalised muscle stiffening
Clonic - rhythmic jerking
Myoclonic - brief jerks
Atonic - loss of tone
Spasms - sudden flexion/extension

20
Q

Prodromal

A

Subjective feeling/sensation
Confusion, irritability

21
Q

Early-ictal

A

Aura
Sensory/cognitive/emotional/behavioural
Focal epilepsy

22
Q

Ictal

A

Depends on seizure
Urinary incontinence and tongue biting

23
Q

Post-ictal

A

Recovery period
Altered consciousness
Todd’s paresis

24
Q

Status epilepticus

A

Seizure > 5 mins, or multiple seizures with incomplete recovery between

Initial management: lorazepam 4mg IV, repeat after 10 mins if no resolution

Clear environment

Tx: IV dextrose, thiamine