Neurology Short Cases Flashcards

1
Q

Test for orientation, Calculation, short-term and long-term memory

A

Orientation: tell time, place, person

Calculation: serial 7s from 100 or serial 3s from 20

Short-term: Repeat 3 objects then test after 5 mins

Long-term: Recall home address, telephone number

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Test for comprehension, expression and repetition of language

A

Comprehension: Follow simple commands

Expression: Name objects

Repetition: Repeat a given phrase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Outline of GCS

Score for good or poor prognosis

A
>11 = good prognosis 
<4 = poor prognosis 

1) Eye opening: spontaneous, to speech, to pain, none
2) Verbal response: Orientated, confused, words, sounds/ grunts, none
3) Motor response to “stick out tongue”: obey command, localize to pain in supraorbital area and hand move up to chin, localize to pain in supraorbital area and elbow flex, Decorticate position, Decerebrate position, none

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Test for sensory inattention

Test for visual inattention

A

Sensory: Touch patient on each upper limb with patient’s eyes closed
Tell which part is touched

Visual: first do visual field test (normal), then ask patient to point to finger which moves on either side of visual field

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Test for bradykinesia?

A

10 second test: flex and extend fingers as quickly as possible, or finger opposition

Wrist rotation as fast as possible

Stomping foot

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Interpret:

  • Slurred speech
  • Deconjugate eye movement
  • Cannot balance, cannot tandem-walk
  • Power normal in UL and LL
  • Fails to do hand clap test
  • Fails to accurately place finger in finger-nose test

Causes?

A

Cerebellar syndrome

  • Dysarthria
  • Nystagmus
  • Intention tremor with past-pointing and dysdiadochokinesia
  • Wide-based, ataxic gait (MUST EXCLUDE MUSCLE WEAKNESS FIRST)

Causes:

1) Cerebellar degeneration: idiopathic, paraneoplastic, familial
2) Toxins and drugs: alcohol, anti-convulsant
3) Cerebellar infarct, hemorrhage, tumor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Investigations for cerebellar syndrome

A

CT/ MRI brain

Serum: paraneoplastic anti-neuronal autoantibodies

CSF: infection and inflammation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Interpret:

Dysphagia +/- hoarseness of voice
Partial ptosis and loss of sweating on left face
Nystagmus towards the left side
Loss of pain and temperature sensation below the face on right
Loss of some facial sensation

Ddx?
Causes?

A

Lateral medullary syndrome

Ddx:
Acute vestibular neuronitis
Benign positional vertigo
focal neurological signs are absent except nystagmus

Causes:
Brainstem infarct from local thrombotic occlusion (Vertebral artery 85%, PICA 15%), arterial thromboembolism (vertebral artery dissection), cardioembolism

Brainstem hemorrhage

Acute brainstem demyelination: MS

Leukoencephalopathy (drugs, hypertension, autoimmune disease)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Interpret:

Impaired visual acuity , afferent pupillary defect with poor direct and consensual pupillary light response

Impaired adduction in one eye with nystagmus in the contralateral eye (nystagmus + deconjugate gaze)

Unsteady and stiff gait, Increased ankle and knee reflexes + bilateral Babinski reflex, weak LL

Some dysarthria intention tremor and post-pointing

Dx?
DDx?

A

Multiple sclerosis: demyelinating disease of CNS, relapsing-remitting symptoms

Optic neuritis
Internuclear opthalmoplegia
Spastic paraparesis
Cerebellar signs

Ddx:
- Neuromyelitis optica
CNS manifestation of rheumatological disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Interpret:

Lack of facial expressions, some drooping saliva, infrequent blinking
Forward flexion of trunk on standing
Soft and monotonous voice
Stiff, shuffling gait with little arm swing
Resting tremor asymmetrical
Slow movement

Dx?
Ddx?
Other motor signs?

A

Parkinson’s disease: degeneration of dopaminergic nigrostriatal neurons (neuromelanin), decrease dopamine activity

Ddx:

  • Progressive supranuclear palsy: no resting tremor
  • Lewy body dementia: hallucination and psychosis in early stage, dementia later
  • Multisystem atrophy: Bilateral cord palsy causing stridor + pyramidal or cerebellar signs
  • Wilson’s disease: young, Kayer- Fleischer ring, limb contractures, psychosis, jaundice
  • Cerebral small vessel diseases - Parkinsonism features
  • Benign essential tremor: Postural tremor symmetrical

Bradykinesia
Power, sensation and deep tendon reflexes preserved

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Interpret:

Symmetrical proximal limb and neck weakness
Muscle tenderness
Normal sensation, no atrophy
+/- Purple heliotropic rash in butterfly distribution over cheeks and eyelids, blanches with pressure

Dx?
Ddx?
Cause?

A

Polymyositis
Dermatomyositis (with purple heliotropic rash)

Ddx:

  • Polymyalgia rhuematica: temporal arteritis
  • Limb girdle muscular dystrophy
  • Myasthenia gravis: fatigable, involves eyes
  • SLE: rash, myositis, photosensitive butterfly rash on face

Cause:
Underlying malignancies: ovarian, pancreatic, breast, nasopharyngeal… etc

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Interpret:

  • Cannot name objects
  • Cannot repeat sentences
  • Can understand fully
  • Non-fluent speech an cannot find right words
A

Expressive dysphasia

Broca area in inferolateral frontal lobe

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Interpret:

  • Cannot understand
  • Fluent speech, fast but words do not make sense

Dx?
Formal term to describe the pattern of speech?

A

Receptive dysphasia

Wernicke’s area in temporal lobe

Paraphasia: forming sentences that don’t make sense
Neologism: forming new words

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Causes of dysphasia?

A

Ischemic stroke*

Hemorrhagic stroke

Dementia: Alzheimer’s, frontotemporal dementia

Encephalitis: HSV

Tumor in relevant area

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

How to accurately test for receptive dysphasia

A

Test with 2-3 stages of command

Partial receptive dysphasia might be able to obey one stage command

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Interpret: (not likely tested)

  • Clawing of fingers
  • Ulcers and scars on hands
  • Wasting of small hand muscles and ulnar area of forearms
  • Some dermatomal loss of pain and temperature sensation of upper limbs
    +/- Horner’s syndrome, kyphoscoliosis, short neck

Dx?
Causes?
Other signs if the brain stem is involved?

A

Syringomyelia (syringobulbia)

Foramen magnum lesion causing expansion of central spinal canal
Spina bifida, tumor, trauma

+/- Diplopia and nystagmus (medial longitudinal bundle)
+/- Facial numbness (trigeminal sensor nuclei)
+/- weakness of SCM and trapezius (XI)
+/- soft palatal paralysis, dysarthria, tongue muscle wasting and fasciculation (XII nuclei)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Describe the lesion that causes syringomyelia

A

Fluid-filled expanded syrinx arising from central spinal cord in the cervical and thoracic regions

Affects decussating fibers of spinothalamic tract + anterior horn of spinal segments + sympathetic fibers at C8/T1 +/- Corticospinal tract

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Interpret:

Flexed right elbow, no movement
Spasticity of right upper arm and weakness
Brisk biceps, supinator and triceps reflexes of right upper limb
Drooling of saliva
Hemiplegic
No cortical signs

A

Cerebral infarction or subcortical hemorrhage - stroke

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Causes of partial ptosis (3)

How to differentiate?

A

Horner’s syndrome: Partial* ptosis, miotic reactive pupil*, anhidrosis, enophthalmos
Myasthenia gravis: Partial ptosis that worsens with gaze, time of day + opthalmoplegia
Partial CNIII palsy: complete ptosis with opthalmoplegia and dilated unreactive pupil

Size and response of pupils

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Interpret:

Complete ptosis of right eye with right dilated pupil in depressed and abducted position

Right efferent pupillary reflex defect
Bilateral afferent responses spared

Dysconjugate eye movement: right eye cannot look up and adduct

A

Complete CNIII palsy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Interpret:

Symmetrical spasticity and weakness of bilateral LL
Brisk knee and ankle reflexes, symmetrical
Clonus in right ankle
Bilateral Babinski reflex
Reduced sensation in all modalities in both lower limbs

A

Spastic paresis caused by thoracic cord lesion (most likely), e.g. vertebral collapse caused by bony metastasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Interpret:

Facial numbness and drooling on right side
Recent URTI
Loss of nasolabial fold on right face
Right upper and lower facial muscle weakness
Cannot close right eyelid
Increase lacrimation from right eye
No loss of sensory sensation

Other signs and symptoms?

A

Right lower motor neuron facial palsy/ right facial nerve palsy/ Bell’s palsy

Loss of taste in anterior 2/3 of tongue and hyperacusis
Examine external auditory meatus and eardrum: exclude otitis media and Ramsay-Hunt syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Difference in epileptic seizure and epilepsy?

A

Epileptic seizure = Brief and unprovoked stereotyped disturbance of behavior, emotion, motor function or sensation due to cortical neuronal discharge

Epilepsy: recurrent unprovoked seizures

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Interpret:

Increased fatigue in general
Increase fatigue in all four limbs 
Double vision, both pupils reactive to light, impaired abduction of right eye
increased fatigue later in the day 
Decreased exercise tolerance from limb weakness 
No dysarthria or dysphagia 
Coherent speech
4/5 muscle power
All reflexes normal 
No cerebellar signs 

Dx?
Test?

A

MG

Tensilon test: IV edophonium ejection
Acetylcholine receptor antibody test
Nerve stimulation test

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

Describe the gait pattern in cerebral stroke, cerebellar stroke and parkinsons

A

hemiplegic gait (stroke),

wide-based ataxic gait (cerebellar),

shuffling, festinating gait with stooped posture and lack of arm swing (Parkinsonism)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

Signs of meningeal irritation/ meningitis

A

→ Brudzinski’s sign: passive neck flexion → hip flexion

→ Kernig’s sign: knee extension with flexed hip → hamstring spasms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

Distinguish between dysphasia, dysarthria and dysphonia

A

□ Dysphasia: disorder in use of language (content)
→ Site: higher centres, hemispheric

□ Dysarthria: difficulty with articulation
→ Site: motor apparatus for articulation and related nerves

□ Dysphonia: altered quality of voice with ↓volume
→ Site: vocal cords and related nerves

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

Causes of dysarthria

A

→ Pseudobulbar palsy: spastic dysarthria
→ Facial weakness: slurred speech
→ Extrapyramidal disease: monotonous speech (due to bradykinesia and rigidity)
→ Alcohol intoxication, cerebellar diseases: loss of coordination, slow/slurred speech

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

Dominant Parietal lobe signs

A

Dominant parietal lobe signs:
→ Acalculia: ask to calculate, eg. serial 7s
→ Agraphia: ask to write
→ Left-right disorientation: ask to show left or right hand
→ Finger agnosia: ask to name each fingers
→ Dysphasias

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
30
Q

Non-dominant parietal lobe signs

A

Non-dominant parietal lobe signs:
→ Sensory and visual inattention/extinction:
- Normal bilateral sensory fields
- Stimuli from one side disappear when two sides are tested together
- Usually tested together with PNS sensory examination
→ Spatial neglect: ask to fill in numbers on an empty clock face
→ Construction apraxia: ask to copy an object you drew
→ Dressing apraxia: ask to put shirt (that has been turned inside out) back on

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
31
Q

Visual field defect in parietal lobe lesion

A

→ Homonymous lower quadrantanopia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
32
Q

Test for CNI

Causes of loss of smell

A

Test smell
□ Place aromatic non-irritant materials close to nose, eg. alcohol swipes

Nasal cavity:
→ URTI (most common)
→ Smoking

Olfactory receptors:
→ Aging

Olfactory bulb and fibres:
→ Ethmoid tumours
→ Basal skull fracture or frontal fracture
→ Pituitary surgery
→ Meningioma of olfactory groove
→ Meningitis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
33
Q

Subsequent tests for visual acuity defects e.g. patient cannot even read first 2 lines

A

□ Can pt count fingers?
□ If no, can pt detect movement?
□ If no, can pt respond to light?

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
34
Q

Correction for refractive error

A

Refractive error should be corrected by pinhole

35
Q

Causes of Acute unilateral vision loss

A

Focal vascular

  • Retinal a. or v. occlusion
  • Temporal arteritis (prominent artery, tender on palpation
  • Non-arteritic ischaemic optic neuropathy

Other focal
- Optic neuritis

36
Q

Causes of acute bilateral vision loss

A

Diffuse vascular
- Bilateral occipital lobe infarct

Diffuse traumatic

  • Bilateral occipital trauma
  • Bilateral optic nerve damage (eg. methyl alcohol poisoning)

Other diffuse
- Somatic conversion disorder

37
Q

Causes of gradual bilateral vision loss

A

Diffuse eye degenerative

  • Cataract
  • Glaucoma
  • Macular degeneration
  • Diabetic neuropathy

Other diffuse chronic

  • Bilateral optic nerve or chiasmal compression
  • Bilateral CN II damage (eg. tobacco amblyopia)
38
Q

Causes of bitemporal hemianopia

A

Lesion at Optic chiasm

  • Pituitary tumour
  • Craniopharyngioma
  • Suprasellar meningioma
39
Q

Causes of homonymous hemianopia

A

No macular sparing = Post-chiasmic lesion

  • Vascular lesions
  • Tumour

With macular sparing = Occipital vascular lesion
- Non-destructive ischaemia at occipital lobe

40
Q

Causes of Homonymous quandrant-anopia

A

Superior quadrant = Temporal Vascular lesions or Tumour

Inferior quadrant = Parietal Vascular lesions or Tumours

41
Q

Causes of ptosis and ectropion

A

Ptosis: dropping of upper eyelid

  • LPS with CN3 and SN component
  • CN3 palsy (complete) vs Horner syndrome (partial)

Ectropion: drooping of lower eyelid

  • Often with eye irritation and watering due to defective drainage
  • D/dx: degenerative, CN7 palsy
42
Q

Which CN are tested in pupillary light reflex?

How to distinguish which nerve has defect?

A

CN2 afferent + CN3 efferent
□ Test direct vs consensual response
□ CN3 palsy: pupil dilates and fixed regardless of light

Swinging flashlight test for relative afferent pupillary defect (RAPD)
→ Paradoxical dilation of affected pupil
→ Shows defect of afferent pathway
→ D/dx: CN2 palsy, unilateral ↓VA

43
Q

How to test for visual accommodation

A

□ Ask pt to look into distance then to a close object (~30cm)
□ Normal: constriction of both pupils

44
Q

Causes of Miosis

A
  • Horner’s syndrome – with partial ptosis, disturbance of sweating
  • Argyll Robertson pupil – small irregular pupils with light-near dissociation
  • Drugs – opioids, parasympathomimetics…
45
Q

Causes of mydriasis

A

Mydriasis (dilated pupil)

  • CN III palsy – with ptosis and ophthalmoplegia
  • Adie’s tonic pupil – with light-near dissociation
  • Ocular causes – eg. iris trauma
  • Parinaud’s syndrome – dorsal midbrain lesion
     Mid-dilated pupils with upgaze palsy
     Light-near dissociation
  • Migraine
  • Drugs – anticholinergic, TCAs, NSAIDs,
    antihistamines, OCs
46
Q

Types and Causes of nystagmus

A

Nysgtamus can be
□ Pendular: equal velocity + amplitude in all directions
□ Jerk: fast phase (specifying direction) + slow phase

□ Jerky horizontal nystagmus: vestibular, cerebellar or central (INO)
□ Jerky vertical nystagmus: cerebellar or central
□ Pendular nystagmus: retinal, congenital

47
Q

Causes of CNIII palsy

A

Midbrain lesion: infarction, demyelination, tumour, basilar aneurysm compression**

Cavernous sinus lesion: with CN IV, V1, VI palsies

  • Tumour
  • Intracavernous aneurysm
  • Cavernous sinus thrombosis

Orbital fissure/orbit lesion: proptosis, CN IV, V1, VI palsies

  • Orbital tumour
  • Periosteitis

Interpeduncular cistern lesion

48
Q

Describe CNIII palsy signs

A
  • Binocular diplopia, worse on contralateral gaze
  • 1o position: abducted + mildly depressed
  • Impaired elevation, depression, adduction
  • Ptosis
  • Mydriatic pupils with impaired/absent pupillary
    light reflex
49
Q

Describe CNIV signs (SO)

A
  • Binocular diplopia, worse on down, contralateral gaze and ipsilateral head tilt
  • 1o position: slightly elevated and extorted
  • Impaired depression upon adduction
  • Head may tilt to opposite side to minimize diplopia
50
Q

Describe CNVI signs (LR)

A
  • Binocular diplopia, worse on ipsilateral gaze
  • 1o position: adducted
  • Impaired abduction
  • Often a/w ipsilateral face-turn
51
Q

How to locate lesion by pattern of sensory/motor loss in CNV

A

Dissociated sensory loss due to separate
locations of trigeminal nuclei:
- Motor at pons
- Light touch at pons

  • Proprioceptive at midbrain
  • Temperature/pain at medulla to C2
52
Q

Test for CNV reflexes

A

Corneal reflex: tests CN V1 (afferent) + VII (efferent)

Jaw jerk:
Normal: slight/no closure of mouth
□ Bilateral UMN V3 lesion: ↑jerk
→ Reason: hyperreflexia in masseter
→ Occurs in pseudobulbar palsy
53
Q

3 trigeminal sensory divisions

A

Opthalmic
Maxillary
Mandibular

54
Q

Test for 5 branches of CNVII motor division

A

□ Temporal (frontalis) → ask pt to look up, following your finger (fix pt’s head when you do it)

□ Zygomatic (orbicularis oculi) → ask pt to close eyes and attempt to open them

□ Buccal (buccinator) → ask pt to blow up the cheeks and try to press on them to feel the tone

□ Marginal mandibular (levator anguli oris) → ask pt to show teeth

□ Cervical (platysma) → ask pt to depress mandible against pressure and feel for platysma tone

55
Q

Signs of CNVII palsy

A

Facial weakness
□ Facial asymmetry
□ Failure to close eyes (orbicularis oculi)
□ Unilateral drooping of corner of mouth (orbicularis oris)
□ Smoothing of facial wrinkles, eg. wrinkled forehead, nasolabial folds

□ Stapedius → ask for hyperacusis
□ Taste of anterior 2/3 of tongue → ask for loss of taste
□ Secretion of lacrimal and oronasal glands → ask for dry eyes and dry mouth

56
Q

UMN and LMN supply of CN VII motor branches

A

□ UMN supply
→ Contralateral to temporal and zygomatic
→ Bilateral to buccal, marginal mandibular and cervical

□ LMN supply → always ipsilateral

57
Q

Signs of CNVIII palsy (3)

A

□ Acute vertigo
□ Hearing loss
□ Tinnitus

58
Q

Test for CNVIII

A

Hearing:
□ Cover opposite ear with finger
□ Rub fingers near ear and ask for response
□ Suspect partial deafness → Rinne’s and Weber’s tests

Rinne’s test:
□ 256Hz vibrating tuning fork on mastoid process
□ No longer hear sound → placed in line with external auditory meatus
□ Rinne-positive = air conduction > bone conduction → normal
□ Rinne-negative = air conduction < bone conduction
→ conductive deafness

Weber’s test:
□ 256Hz vibrating tuning fork on centre of forehead
□ Ask pt to locate source of sound
□ Normal → central
□ Sensorineural deafness → contralateral deviation
□ Conductive deafness → ipsilateral deviation

59
Q

Causes of conductive hearing loss (not exhaustive)

A

Trauma: tympanic membrane rupture, ossicular disruption

Infection: Otitis media, cholesteatoma

Wax

Otosclerosis tumors

60
Q

Causes of Cochlear sensorineural loss (not exhaustive)

A

Congenital: aplastic maternal rubella

Trauma: petrous temporal fracture

Infections: Mumps, measles, meningitis

Drugs: Streptomycin

61
Q

Causes of vertigo (not exhaustive)

A

Trauma

Suppurative labyrinthitis

BPV

Meniere’s disease

Vestibular neurontiis

62
Q

Features of CN IX palsy

A
  • Sensory loss in oropharynx
  • Loss of gag reflex
  • Dysphagia
63
Q

Features of CNX palsy

A
  • Palatal weakness:
     Unilateral – minimal
     Bilateral – nasal regurgitation of fluid, hypernasality
  • Pharyngeal weakness:
     Unilateral – drooping wall on affected side
     Bilateral – marked dysphagia
  • Laryngeal weakness:
     SLN – unable to sing high pitch
     Unilateral RLN – choking, hoarseness
     Bilateral RLN – airway obstruction
64
Q

Test for CNIX and CNX palsy

A

Inspection:
□ Ask pt to open mouth and say ‘ah’
□ Use tongue depressor to depress tongue
□ Normal: soft palate rise symmetrically with no uvula deviation
□ CN X palsy: uvula deviated to normal side (unopposed musculus uvulae)

Gag reflex: tests CN IX (afferent) and CN X (efferent)
□ Touch palate/pharynx/tonsil on one side until ‘gagging’
□ Compare sensitivity on each side
□ Normal: bilateral palatal contraction
□ Absent: CN IX or CN X palsy

Other signs:
□ Hoarseness: ask pt to speak then to cough
→ Characteristics ‘bovine cough’ in RLN lesions
□ Dysphagia: ask pt to swallow water

65
Q

Test for CNXI

A
Trapezius:
□ Ask pt to shrug shoulder
□ Feel bulk of trapezius muscles
□ Attempt to push shoulders down
□ CN XI palsy → weakness

Sternocleidomastoid:
□ Ask pt to turn head to the side against resistance
□ Feel bulk of sternocleidomastoid
□ CN XI palsy → wasting

66
Q

Test for CNXII

A

□ Difficulty in swallowing
□ Sensation of choking if tongue slips back into throat

Inspection:
□ Ask pt to open mouth and inspect the tongue
→ Atrophy (↑folds, wasting) = LMN lesion
→ Fasciculation (small wriggling movements) = LMN lesion (normal if happens in protrusion)

□ Ask pt to protrude tongue
→ Deviation → ipsilateral LMN lesion

67
Q

Features of UMN and LMN lesions in CNXII

A

□ UMN lesion:
→ Unilateral → no S/S
→ Bilateral → small, immobile (spastic) tongue

□ LMN lesion:
→ Unilateral → fasciculation, wasting and weakness
→ Bilateral → dysarthria

68
Q

Signs of LMN lesion in upper or lower limbs

A

Hypotonia
Fasciculation
Hyporeflexia

69
Q

How to distinguish UMN lesion from cerebellar lesion using extended arms

A

Ask pt to hold hands out with palms facing up and close eyes
□ UMN lesion → pronator drift (sensitive sign)
(arm gradually pronates and drifts downward)

□ Cerebellar lesion → slow upward + pronation drift

□ Proprioceptive defect → finger random movement

70
Q

Signs of extrapyramidal lesions e.g. Parkinson’s

A

→ ‘Lead-pipe’ rigidity: steady ↑resistance throughout movement

→ ‘Cog-wheel’ rigidity: ‘lead-pipe’ + tremor

71
Q

MRC muscle power grading?

A

0 – no movement
1 – flicker of contraction w/o movement
2 – movement possible but not against gravity (i.e. horizontal movement)
3 – movement against gravity

4- – slight movement against resistance
4 – moderate movement against resistance
4+ – submaximal movement against resistance

5 – normal power

72
Q

All upper limb motor tests and corresponding spinal levels

A

Shoulder abduction
(C5-6)
Shoulder adduction
(C6-8)

Elbow flexion
(C5-6)
Elbow extension
(C7-8)

Wrist flexion
(C6-7)
Wrist extension
(C7-8)

Finger flexion
(C7-8)
Finger extension
(C7-8)

Finger abduction
(C8-T1)
Finger adduction
(C8-T1)

Thumb opposition
(C8-T1)
Thumb abduction
(C7-8)

73
Q

Spinal levels for all upper and lower limb reflexes

A
  • Ankle jerk – S1-2
  • Knee jerk – L3-4
  • Biceps/supinator jerk – C5-6
  • Triceps jerk – C7(-8)
  • Hoffman reflex – C(7-)8
74
Q

Bicep jerk level, nerve

A
Bicep jerk (C5-6):
□ Nerve: musculocutaneous n., biceps tendon
75
Q

Supinator jerk level, nerve, location

Normal vs abnormal jerk?

A
Supinator jerk (C5-6):
□ Nerve: radial nerve, Place finger ~10cm from base of thumb

□ Look for: elbow flexion
□ Finger flexion + elbow extension = inverted supinator jerk
→ Characteristic of spinal cord lesion at C5-6
→ C5-6 LMN lesion → no supinator and bicep jerks

76
Q

Triceps jerk level, nerve

A
Triceps jerk (C7-8, C7 major):
□ Nerve: radial nerve, few inches above olecranon at triceps tendon
77
Q

Test for upper limb spinothalamic and DCML pathways

A

Spinothalamic: pinprick for pain sensation with orange stick

DCML: Vibration with 128Hz tuning fork at DIP, wrist, olecranon, shoulder
Proprioception by moving thumb with pt eyes closed

78
Q

4 patterns of sensory loss

A

□ Dermatome → spinal cord or nerve root
□ Single peripheral nerve territory → peripheral nerve
□ Glove-and-stocking distribution → peripheral neuropathy
□ Hemisensory loss → unilateral spinal cord, upper brainstem, thalamus, cerebral

79
Q

Features of upper limb miscoordination

A

Finger-nose test: Cerebellar signs may present as
→ Dysmetria (past-pointing): over-shooting or under-shooting
→ Intention tremor: increasing tremor when target is approached

Rapidly alternating movements: dysdiadochokinesia

Rebound: Excessive swinging and failure to return into original position

80
Q

Test for lower limb tone

A

Lift the leg suddenly with both hands in popliteal fossa: ↑tone → leg kicks upward with heel leaving the bed

Ankle clonus: Hyperreflexia = persistent oscillatory movement

81
Q

All tests for lower limb power

A
Hip flexion (L1-2)
Hip extension (L5-S1)
Hip adduction (L2-3)
Hip abduction (L4-5)
Knee extension (L3-4)
Knee flexion (L5-S1)
Dorsiflexion (L4-5)
Plantar flexion (S1-2)
Toe extension (L5)
Ankle eversion (L5-S1)
Ankle inversion (L5-S1)
82
Q

Locations for LL dermatomes

A
L1: Mid-inguinal point 
L2: Mid thigh 
L3: Medial epicondyle 
L4: Medial malleolus 
L5: 3rd MTP 
S1: Heel 
S2: popliteal fossa 
S3: buttock
83
Q

Tests for LL coordination

A

Heel-shin test: Cerebellar disorder = clumsiness

Rhomberg test:
- Check balance with eyes open: Cerebellar ataxia = poor balance or excessive swaying (‘negative’ Rhomberg test)
- Check balance again with eyes closed: Sensory ataxia (poor proprioception) = poor balance or excessive swaying
(‘positive’ Rhomberg test)

Gait: tandem (heel-to-toe) walking, gait ataxia (cerebellar sign)