Neurology Flashcards

1
Q

Features of essential tremor

A

Essential tremor (previously called benign essential tremor) is an autosomal dominant condition which usually affects both upper limbs

Features
➡️5-10hz (Parkinson’s 3-5hz)
➡️Always bilat
➡️postural tremor: worse if arms outstretched
➡️improved by alcohol and rest
➡️most common cause of titubation (head tremor)
➡️No micrographia

Management
➡️propranolol is first-line
➡️primidone is sometimes used

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2
Q

Scoring system if previous TIA to predict stroke risk

A
Age >= 60  --------->1
BP >=140/90 ------> 1
Clinical features 
   Speech disturbance, no weakness --->1
   Unilat weakness ---->2
Duration 10-59min ---->1
                >60min ------>2
Diabetes --------------->1

0-7
>4 is high risk

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3
Q

Management from abcd2 scores

A
High risk >4 
300mg aspirin daily immediately
Specialist assessment and investigation within 24hr
below 4 
assessment within 1wk

but if 2 TIAs or more in a week, then HIGH RISK

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4
Q

OSCES description of Parkinson’s

A

Parkinson’s disease is a progressive neurodegenerative condition caused by degeneration of dopaminergic neurons in the substantia nigra.. This results in a classic triad of features: bradykinesia, tremor and rigidity. The symptoms of Parkinson’s disease are characteristically asymmetrical.

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5
Q

Drug induced Parkinson’s vs Parkinson’s disease

A

Drug-induced parkinsonism has slightly different features to Parkinson’s disease:
➡️motor symptoms are generally rapid onset and bilateral
➡️rigidity and resting tremor are uncommon

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6
Q

Symptom presentation of Parkinson’s disease indicating prognosis (from Majeed teaching)

A

PD has a Better prognosis if in a woman (about twice as common in men), or if presents with tremor symptoms first

There is a Worse prognosis if presents with rigidity first

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7
Q

Presenting symptoms of MS

A

Commonest presenting symptoms (nearly all have fatigue too)
➡️Limb weakness 40%
➡️Optic neuritis 22% (classically greying monocular visual loss with colour desaturation and painful eye movements -this often precedes visual loss)
➡️Parasethesia 21%
➡️Diplopia 12%
➡️Vertigo 5%
➡️Trigeminal neuralgia 2% (rarely presenting complaint but is seen more in MS patients)

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8
Q

What is Uhthoff’s

A

Seen in MS. Specifically visual loss after exercise (but often just referred to as after any heat, eg hot bath)
Previous optic neuritis causing heat dependent visual loss

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9
Q

What is L’Hermittes?

A

Symptom seen in MS
➡️Electrical shock paraesthesia down limbs when stretch
➡️Due to previous demyelination of cervical cord, so they become mechano-sensitive

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10
Q

Definition of relapse in MS

A

(?check)

New neurological disturbance which lasts longer than 24 hrs (they usually last 6wk)

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11
Q

Diagnosis of MS

A

At least TWO neurological events separated by time and space

So➡️ exclude mimics (sarcoidosis, hiv, lupus)
➡️ MRI looking for dawsons fingers, ventricular dilation, cerebral atrophy
➡️ LP with inflam, oligoclonal bands (positive in95%, not specific)
➡️ visually evoked potential, look for delay

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12
Q

Signs of cerebellar damage

A
Dysdiadochokinesia 
Ataxia
Nystagmus
Intention tremor
Slurred speech
Hypotonia
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13
Q

Peripheral neuropathy

A
Alcohol
B12
Chronic renal failure
Diabetes and drugs (tb meds etc)
Every vasculitis
Cancer (paraneoplastic), lymes and Charcot Marie tooth
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14
Q

Who needs ct head after head injury?

A

If any of the following are present, a CT is required immediately:
➡️GCS once

Loss of consciousness AND any of the following:
➡️Age ≥65
➡️Coagulopathy
➡️’Dangerous mechanism of injury’, eg car crash or fall from great height
➡️Anterograde amnesia of >30min

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15
Q

When might you get ‘claw hand’? And what other signs?

A

Ulnar nerve palsy (claw hand is due to loss of lumbrical innervation)
Weak pincer grip
Loss of sensation on fifth finger and ulnar half of fourth finger
Wasting of first dorsal interosseous muscle

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16
Q

Causes of carpal tunnel syndrome…

A
Rheumatoid arthritis
Acromegaly
Pregnancy
Idiopathic
Diabetes
Trauma
Tenosynovitis of flexor tendons
Thyroid (hypo)
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17
Q

Upper limb nerve roots for movements

A
Shoulder abduction C5
Elbow flexion C6
Wrist extension C7 (cock wrist back)
Finger extension C8 (fingers back)
Finger abduction T1 (spread fingers)
18
Q

Drugs that are associated with idiopathic intracranial hypertension

A
tetracycline antibiotics
isotretinoin
contraceptives
steroids
levothyroxine
lithium
cimetidine
19
Q

Features of Parkinsonial gait

A
Shuffling
Hesitancy
Festinating (Latin for hurry)
Reduced arm swing
Flat foot strikes (instead of heel to toe)
Freezing of gait
20
Q

Causes of SAH

A

80% are rupture of berry aneurysm (assx with PKD, ehlers danlos, coarctation)
Rest are AV malformations
Trauma
Tumour

21
Q

Investigation for SAH

A
CT negative in 5%
So LP (but wait 12hr for xanthochromia to develop)
22
Q

Management of cerebral oedema

A

Hyperventilation

- the decreased CO2 reduces cerebral blood flow

23
Q

Reversible cause of dementia to rule out

A

Normal pressure hydrocephalus
Thought to be secondary to decreased CSF absorption in arachnoid villi
- enlarged fourth ventricle

24
Q

Triad of normal pressure hydrocephalus

A

Gait abnormalities (like PD)
Urinary incontinence
Dementia / bradyphrenia (slowness of thought)

25
Q

Management of normal pressure hydrocephalus

A

Ventriculoperitoneal shunting

26
Q

Causes of carpal tunnel

A
Myxoedema
Edema HF
Diabetes
Idiopathic
Acromegaly
Neoplasm
Trauma
RA
Amyloidosis
Pregnancy
27
Q

Contraindications to LP

A

Raised ICP (unless just idiopathic intracranial hypertension)
Coagulopathy
Infection at needle site
…no consent!

28
Q

Complications for LP

A

Headache….common, lie down for two hours afterwards
Parasthesia
Permanent nerve damage is very rare

29
Q

CSF analysis - bacterial vs TB

A

Both will have low glucose, high protein
Bacterial is cloudy (tb may be slightly)
Bacterial will have polymorphs (tb will be lymphocytes)

30
Q

International migraine criteria

A
At least 5 of
Between 4 and 72hr
Characteristic (unilat, puls, mod/severe, worse with activity)
During get: N/V, Photo/phonophobia
Exclude other causes
31
Q

Features of neurofibromatosis type 1

A

Lack of neurofibromin (tumour suppressor)
Over 6 cafe au lait (over 15mm)
Axillary or inguinal freckles
Two or more neurofibromas
Two or more Iris harmatomas (Lische nodules)
First degree relative
(Also may have scoliosis)

32
Q

Managment of mild moderate alzheimer’s

A

NICE now recommend the three acetylcholinesterase inhibitors (donepezil, galantamine and rivastigmine) as options for managing mild to moderate Alzheimer’s disease

33
Q

Drugs that cause Parkinsons

A
Atypical antipsychotics
Calcium channel blockers 
Amiodarone
Typical antipsychotics
Lithium
metoclopramide
34
Q

Management of GBS

A

Immunoglobulins, monitor FVC every 4 hours and ventilate if under 1.5 or if O2 under 10

35
Q

Diagnosis of GBS

A

Suggestive hx, (progressive weakness of all 4 limbs, areflexia, Mild sensory involvement, Absence of fever, no other diagnosis (MG, botulism, poliomyelitis etc))

CSF with HIGH protein and low WCC (under 10)

36
Q

Predominantly motor polyneuropathies

A

GBS, lead poisoning, Charcot Marie tooth

37
Q

Young patient with acute neck pain and hemiplegia.. Diagnosis

A

Carotid artery dissection (remember, tunica intima and tunica media split making false lumen). Common cause of stroke in young patients, may have neck pain or headache

38
Q

Antibiotic contraindicated in myasthenia gravis

A

Aminoglycosides (Gentamicin)

39
Q

Presentation of venous sinus thrombosis

A

Young patient headache seizure paresis papilloedema
Ct string sign
Mx heparin

40
Q

What vitamin deficiency causes dermatitis, diarrhoea and dementia?,

A

Vitamin B3, aka Niacin deficiency (diagnosis is Pellagra)