Neuro - symptoms + signs Flashcards

1
Q

Meningitis - symptoms + signs

A
  • Non-specific features
  • fever, headache, N+V, lethargy, irritability, muscle/joint pains, refusing food, respiratory symptoms
  • Stiff neck
  • Non-blanching/purpuric rash
  • Back ridgidity
  • Photophobia
  • Altered mental state
  • Kering’s sign - pain + resistance on passive knee extension with hips fully flexed
  • Brudzinski’s sign - hips flex on bending the head forward
  • Paresis, focal neurological defcits (incl cranial nerve involvement, abnormal pupils)
  • Seizures, LOC
  • Shock (tachy, hypotension, resp distress, poor urine output, increased cap refill time, altered mental state, leg pain, cold hands + feet, unusual colour)
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2
Q

Subdural haemorrhage signs and symptoms

A
Fluctuating consciousness
Confusion
Personality changes
Symptoms of increased ICP
Can present as UMN signs (e.g. pronator drift)
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3
Q

Main difference between meningitis + encephalitis

A

In meningitis consciousness is not impaired where is in encephalitis it is usually always affected

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4
Q

Anterior cerebral artery stroke symptoms + signs

A

Contralateral hemiparesis lower limb>upper limb
Behavioural changes

https://doctorlib.info/anatomy/clinical-neuroanatomy-28/clinical-neuroanatomy-28.files/image227.jpg

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5
Q

Middle cerebral artery stroke symptoms + signs

A

Contralateral hemiparesis upper limb/face>lower limb
Contralateral hemisensory loss (makes sense because somatosensory cortex in the parietal lobe is affected)

Apraxia (bc parietal lobe is affected - involved in bringing together + combining information needed to perform skillfull actions)

Receptive/expressive aphasia (involvement of Wernicke’s + Broca’s areas)
Broca’s area - expressive aphasia, broken speech
Wernick’s area - receptive aphasia
(optic radiation contains tracts that carry information from the lateral geniculate nucleus to the primary visual cortex in 2 loops: Meyer’s + Baum’s)

Quadrantanopia
Superior optic radiation (Baum’s loop) - parietal lobe, causes contralateral inferior quadrantopoia
Inferior optic radiation (Meyer’s loop) - temporal lobe, causes contralateral superior quadrantopoia

Hemineglect (parietal lobe)
Facial weakness

https://doctorlib.info/anatomy/clinical-neuroanatomy-28/clinical-neuroanatomy-28.files/image227.jpg

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6
Q

Posterior cerebral artery stroke symptoms + signs

A

Contralateral homonymous hemianopia
(often damage to the occipital lobe/visual cortex leads to macular sparring - large macular representation, dual blood supply (PCA, MCA))

Visual agnosia (damage to the visual association cortex)

https://doctorlib.info/anatomy/clinical-neuroanatomy-28/clinical-neuroanatomy-28.files/image227.jpg

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7
Q

Brainstem damage in stroke

A

Reduction in consciousness
Cranial nerve pathology
IPSILATERAL SIGNS

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8
Q

Cerebellar stroke

A

DANISH

Dydiadochochenesia
Ataxia
Nystagmous
Intention tremor
Slurred speech
Hypotonia

IPSILAERAL SIGNS

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9
Q

Total anterior circulation stroke (TACS) vs Partial anterior circulation stroke (PACS)

A

Contralateral motor or sensory deficit
Homonymous hemianopoia
Higher cortical dysfunction (e.g. aphasia)

TACS - all 3 of them
PACS - any 2 of them

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10
Q

Posteror circulations stroke

A

Any of:
Isolated homonymous hemianopoia
Brainstem signs
Cerebellar ataxia

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11
Q

Lacunar stroke (LACS)

A

Any of
Pure motor deficit
Pure sensory deficit
Sensorimotor deficit

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12
Q

Cauda equina presentation

A

LMN symptoms (nerve roots affected and not the CNS so no UMN signs as in spinal cord compression)
Perianal anaesthesia
Bladder retention
leg weakness

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13
Q

Lacunar infarct affecting the

o Affecting the internal capsule/pons

A

Internal capsule - Pure motor, pure sensory, mixed motor + sensory signs

Pons - dizziness/vertigo, ataxia

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14
Q

Lacunar infarct affecting the

o Affecting the thalamus

A

loss of consciousness, hemisensory deficit

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15
Q

Lacunar infarct affecting the

o Affecting the basal ganglia

A

Dyskinesias

hemichorea, hemiballismus, parkinsonism

Intact cognition/consciousness

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16
Q

Lacunar infarct affecting the

o Multiple lacunar infarcts

A
Vascular dementia
Urinary incontinence
Gait apraxia
Shuffling gait
Normal or excessive arm-swing
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17
Q

Normal pressure hydrocephalus signs - popular SBA

A

Hakim’s triad (weird walking water)

  • Urinary incontinence
  • Dementia
  • Gait disturbance (ataxia, shuffling)(also cognitive impairement, hyperreflexia)
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18
Q

Hydrocephalus symptoms + signs

Acute onset

A
Papilledema
Headache
Vomiting
Impaired upward gaze
Sunset eyes
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19
Q

Hydrocephalus symptoms + signs

Gradual onset

A
  • Unsteady, slow, cautious gait
  • Unsteady gait (Levodopa-unresponsive gait apraxia (spasticity in legs))
  • Large head
  • Unilateral/bilateral 6th nerve palsy (2o to raised ICP)
  • Double vision
  • CN palsies
  • Cognitive impairement
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20
Q

Multiple sclerosis symptoms + signs MS

A
CNS so UMN signs
Visual
- Blindness/hemianopoia
- Optic neuritis
- Scotoma
- Symmetrical HORIZONTAL jerking nystagmus
- LR weakness - may cause double vision
- Eye pain commonly exacerbated on eye movement as the inflamed optic nerve sheath is stretched
- INO (intranuclear ophthalmoplegia)

Face

  • Bell’s palsy
  • Trigeminal neuralgia
  • Paroxysmal dysarthria

Ears

  • Deafness
  • Unsteadiness

Autonomic system

  • Bladder - urgency, frequency, incontinence, impaired bladder emptying
  • Sexual problems - impotence
  • Loss of thermoregulation - excess sweating

Cognitive

  • Visual + auditory attention affected
  • Loss of memory

Perineum + genital numbness, altered sphincter function –> characteristic feature of MS

intention tremor, ataxia, dysmetria - cerebellar signs
Lhermitte’s sign = electric shock sensations
MS with cervical posterior column involvement
Sudden neck flexion causes electric-shock sensations to the limbs

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21
Q

Motor neurone disease symptoms MND

A

MND=ALS

  • UMN + LMN dysfunction

Oculomotor + sphincter functions spared!!

Limb onset more most common (usually upper limbs)

  • Pt drop objects, can’t manipulate objects with one hand
  • Wasting of intrinsic muscles
  • Fasciculations

Lower limb problems

  • Foot drop
  • Gait disorder
  • Difficulty rising from low chairs + climbing stairs (+ wasting, fasciculation, change in tone + reflexes unlike MG)

Progressive ASYMMETRICAL weakness of bulbar, limb, thoracic, abdominal muscles
Onset can also be bulbar (20%) - slurring of speech, emotional lability, dysphagia, wasting + fascisulation of tongue
Onset can rarely be respiratory - dyspnoea, orthropnoea, hypoventilation overnight (unrefreshing sleep, early morning headahces)

NO sensory involvement

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22
Q

Course of disease in myasthenia gravis

A

Starts in the eyes with weakness to the extrinsic ocular muscles and LPS

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23
Q

Myasthenis gravis symptoms

A
  • Muscle weakness that increases with exercise and improves with rest
  • Fatiguable muscles
  • Ptosis (but pupils are spared unlike in Horner’s syndrome where there is miosis)
  • Double vision
  • Oropharungeal/appendicular weakness
    Dysphagia, dysarthria
    Reading aloud may provoke dysarthria of nasal speech after 3 mins

Proximal limb weakness
- difficult in getting out of chairs, climbing stairs but no muscle wasting, no fasciculations, normal tone, normal reflexes, normal sensation unlike MND

  • SOB

NO sensory signs
Weakness is greater in proximal muscles (rather than distal as in GBS) + commonly involves spinal nerves

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24
Q

Median nerve damage symptoms

A
  • Wasting of the thenar muscles
  • Lack of ability to abduct + oppose the thumb
  • Weakness in forearm pronation + wrist + finger flexion
  • Sensory loss in thumb, index, middle finger + radial aspect of ring finger
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25
Ataxic gait what is it a sign of? Where is it seen?
Cerebellar sign Seen in Wernicke's encephalopathy
26
Hemiplegic gait sign
Typically following a stroke
27
Shuffling gait sign
PD
28
Scissor gait sign
``` Cerebral palsy cord lesions (e.g. MS) ``` results from increased spasticity in both legs
29
Choreiform gait sign
Huntington's
30
Wernicke's encephalopathy triad
- Ophtalmoplegia - Confusion - Ataxia
31
Wernicke's encephalthy triad vs NPH triad vs encehalitis
Wernicke's encephalopathy - Eye signs - ophthalmoplegia, nystagmus, diplopoia - Confusion - Ataxia (due to cerebellar damage) NPH triad (Hakim's triad) - Urinary incontinence - Dementia - Gait disturbance (ataxia, shuffling) Encephalitis - Fever - Headache - Altered mental status
32
Basal skull fracture signs
haemotympanum panda eyes CSF leakage from ear or nose Battle's sign
33
Guillaine Barre syndrome symptoms GBS
``` PNS so LMN signs Weakness, paraesthesia and hyporeflexia Progresses acutely SYMMETRICAL I fasciculation T flaccid tone P ascending pattern of progressive SYMMETRICAL weakness starting at the lower extremities affects proximal before distal muscles R hyporeflexia or absent S neuropathic pain, back pain, sensory abnormalities usually mild ``` Autonomic symptoms - decreased sweating, decreased heat intolerance, tachycardia, HTN, postural hypotension, ileus, urinary retention Face - Facial weakness - facial droop, facial nerve palsy, Dysphasia, dysarthria Extra-ocular muscle weakness - Diplopoia Bulbuar dysfunction causing oroharyngeal weakness - Dysphagia
34
Trigeminal neuralgia symptoms + signs
- Paroxysms of Sudden, Unilateral, Stabbing/electric-shock like pain - Most common in 2nd + 3rd divisions of the trigeminal nerve - Does not interfere with sleep - Following an episode of pain there is a refractory phase of several minutes during which there will not be another paroxysm of pain even if the triggering stimulus recurs - Autonomic symptoms - lacrimation +/- redness of eye - Progressive increase in frequency, duration, severity of attacks
35
Encephalitis symptoms
o Meningism (photophobia, neck stiffness, headache) ``` Followed by: o Altered state of consciousness o Seizures o Personality changes o Cranial nerve palsies o Speech problems o Motor + sensory deficits o Focal neurological signs (hemianopia, aphasia, hemiparesis, ataxia, brisk tendon reflexes, babinski's signs, CN deficits) o Increased ICP ```
36
Triad of encephalitis
- Fever - Headache - Altered mental status Cognitive dysfunction Memory disturbances Psychiatric + behavioural manifestations (hallucinations, withdrawal apathy, personality changes)
37
What do we mean by meningism?
o Photophobia o Neck stiffness o Headache
38
BPPV symptoms + signs
• Vertigo Sudden onset Severe Brief duration - <30s Episodic Rapid resolution if the head is kept still Brief latent period 5s-20s between the provocative movement + the experience of vertigo * Specific provoking positions - looking up, bending down, getting up, turning head, rolling over in bed to one side * Symptoms worse in the mornings * Nausea, imbalance, light-headedness • Positive Dix-Hallpike/Nylen-Barany manoeuvre – posterior canal BPPV o Positive test – reproduction of vertigo + nystagmus o Nystagmus - Torsional – L ear has a clockwise torsional nystagmus response, R ear has an anti-clockwise response, horizontal nystagmus suggests horizonal canal BPPV - Reversible with seating - Fatigable with repeat testing - Occurs with 1-5s latency - Lasts <30s • Positive supine lateral head turn – lateral canal BPPV o Positive test – vertigo + nystagmus o Horizontal nystagmus without torsional component o When head is rotated towards the affected side the nystagmus will beat towards the ground (geotropic + be more intense) * Normal neurological examination * Normal otological examination
39
Meniere's triad
``` - Vertigo m to h N+V attacks tend to cluster in groups - Unilateral Hearing loss - Unilateral Tinnitus ``` Not provoked by positional changes
40
Meniere symptoms + signs
Triad - Vertigo m to h N+V attacks tend to cluster in groups - Unilateral Hearing loss - Unilateral Tinnitus - Unilateral aural fullness - Positive Romberg's test - Fukunda's stepping test o Turning towards the affected side when asked to march in place with eyes closed
41
Type 1 neurofibromatosis symptoms + signs | NF
- Painless mobile lumps under the skin (SC neurofibromatomas may be tender to touch + cause tingling in the distribution of the affected nerve) - Cafe au lait spots - back, buttocks, thighs - Lisch nodules on iris - Spinal scoliosis - RAS - Phaeochromocytomas * Large neurofibromas can develop in the abdominal cavity + press against nearby organs and impair their function (e.g. kidneys, constipation, abdominal pain) * Optic gliomas (15%) – visual acuity loss, abnormal colour vision, visual field loss [most common presentation is asymmetrical visual fields] * Disruption of bone maintenance and reduced bone mineral density – possibility of osteoporosis * Most common additional manifestations: LEARNING DISABILITIES, optic pathway gliomas, diffuse plexiform neurofibromas, dystrophic SCOLIOSIS, sphenoid wing dysplasia, renovascular hypertension, malignant nerve sheath tumours, SHORT STATURE * Also risk of seizures, bone dysplasia, Congenital heart disease (PS, HTN), Pheochromocytoma, RAS
42
Type 2 neurofibromatosis symptoms + signs
* BILATERAL acoustic neuromas (acoustic neuromas can occur in individuals that don’t have neurofibromatosis but in neurofibromatosis type II they tend to occur bilaterally) – tinnitus, gradual hearing loss on both sides, +/- loss of balance, facial weakness due to vestibular schwannomas --> SENSORINEURAL HEARING LOSS * Intracranial meningiomas * Spinal gliomas – pain, numbness, weakness (compression of the spinal cord) * Paraspinal schwannomas * Cataracts (Posterior subcapsular lenticular opacities) * Hamartomas in the retina * Absence of café-au-lait spots symptomatic by age 20
43
Huntington's symptoms
``` Chorea Athetosis - writhing movements of hands, early in course of disease pt can mask involuntary movements by incorporating them into socially acceptable movements .e.g. twiddling thumbs Ataxia Loss of coordination + balance Deficit in fine motor coordination Dysarthria, dysphagia ``` Cognitive decline Impaired work or school performance Personality changes - irritability, impulsativity, temper outbursts, loss of enthusiasm or involvement in previously engaging activities, self-neglect, depression Dementia
44
Parkinson's disease cardinal features PD
- Bradykinesia - Rigidity - Lead pipe, cogwheel rigidity - Postural instability - seen late, lack of ability to voluntarily adjust position in response to postural disturbance - Resting tremor - 3-4 hz, pill rolling, can be induced by concentration, absent with activity
45
Parkinson's disease symptoms PD
- Tremor at rest (can be induced by concentration, absent with activity, Low frequency – 3-4 Hz, pill rolling) - Rigidity - Lead pipe, cogwheel rigidity - Bradykinesia - Postural instability - seen late, lack of ability to voluntarily adjust position in response to postural disturbance 5Ms - Hypomimic face/masked facies - Monotonous speech/hypophonia - Micrograpia - Misery - depression - Memory loss - dementia - Marche a petit pas* - Stooped posture - Shuffling gate - Difficulty rising from a sitting position + starting to walk - Small shuffling steps, unsteadiness on turning (taking several steps to turn), difficulty in stopping* Neuropsychiatric: hallucinations, anxiety, confusion, stupor, impulsivity, depression, cognitive decline, dementia, paranoia, visuospatial dysfunction Autonomic + Vegetative: bladder, bowel, hypotension, Impotence, dysarthria, dysphagia, drooling, rash, anosmia Sleep: restless legs, REM sleep disorder, nightmares
46
Parkinson's disease signs
4 cardinal signs - Bradykinesia - Rigidity - Lead pipe, cogwheel rigidity - Postural instability - seen late, lack of ability to voluntarily adjust position in response to postural disturbance - Resting tremor - 3-4 hz, pill rolling, can be induced by concentration, absent with activity - Lack of arm swing when walking
47
SAH symptoms
- Thunderclap headache Peaks within 1-5mins Lasts more than 1h - N+V - Photophobia - Non focal neurological signs - Depressed/loss of consciousness or confusion – caused by blockage of the normal CSF circulation by blood in the subarachnoid space - Isolated pupillary dilation with loss of light reflex may indicate bran herniation as a result of rising intracranial pressure - if blood irritates the meninges - signs of meningismus present (neck stiffness, photophobia)
48
Symmetrical or asymmetrical symptoms MND GBS
MND - asymmetrical | GBS - symmetrical
49
Difference between Vasovagal syncope Arrhythmias Strokes-Adam attack Epilepsy
Vasovagal (reflex) - Precipitating factor - Sweating - Nausea - Pale - Dizzy - Narrowing of visual fields - May twitch + be incontinent - Seconds - Quick recovery on sitting Arrhythmias (cardiac) - Chest pain - Palpitations - Seconds - Quick recovery on sitting ``` Strokes-Adam attack (cardiac - transient arrhythmias cause a drop in CO and LOC, underlying problem - complete heart block or sinoatrial disease) - Pale - Seconds - Facial flush (treatment is pacemaker) ``` Epilepsy - Aura or no warning - <3 mins - Tongue biting - Twitching - Incontinence - Slow recovery - Post-ictal Confusion/Headache/Myalgia
50
Difference between an aura + a prodrome
Aura - part of the seizure - can last up to a few minutes - strange smells, flashing lights, deja vu etc - suggests that the epilepsy is focal Prodrome - not part of the seizure - can last up to a few hours - change in the patient's experience or mood
51
What is Tood's paresis?
- Syndrome assosciated with weakness or paralysis of part/all the body - Happens after focal-onset seizure
52
Focal seizure - Frontal lobe epilepsy symptoms + signs
- Motor symptoms - Jacksonian march - muscular spasm spreads from distal part of the limb to a larger area of the body - Post-ictal flaccid weakness (Todd's paralysis) - Disinhibition --> Involuntary actions
53
Focal seizure - parietal lobe epilepsy
Sensory disturbances (pain, tingling, numbness)
54
Focal seizures - occipital lobe epilepsy
Visual disturbances (spots, lines, flashes)
55
Focal seizures - temporal lobe epilepsy
- Aura (epigastric discomfort) - Automatisms (playing with fingers, lip smacking) - Hallucinations - Olfactory hallucinations also called complex partial seizures
56
Exertional syncope sign of
AS, HOCM HOCM - L ventricular outflow obstruction due to asymmetrical septal hypertrophy - occludes the outflow tract during systole
57
What is the Miller-Fischer syndrome and what are the signs and symptoms?
Variant of GBS Triad of - Ophthalmoplegia - Areflexia - Ataxia but no muscle weakness
58
Brown sequard syndrome What is it describe the symptoms
Occurs when the spinal cord is injured on one side much more than the other Lateral corticospinal tract crosses over in the medulla (motor) Dorsal columns cross over in the medulla (sensation, vibration, proprioception) Spinothalamic tract crosses over in the spinal cord (pain+temperature) Therefore - Ipsilateral loss of motor function, sensation, vibration, proprioception - Contralateral loss of pain + temperature
59
Crossing + function of Lateral corticospinal tract Anterior corticospinal tract Dorsal columns cross Spinothalamic tract crosses
Lateral corticospinal tract crosses over in the medulla (motor to distal digits, limbs) Anterior corticospinal tract crosses over in the spinal cord (motor to proximal muscles of the trunk) Dorsal columns cross over in the medulla (sensation, vibration, proprioception) Spinothalamic tract crosses over in the spinal cord (pain+temperature)
60
Difference and similarities between spinal cord compression + cauda equina syndrome
Spinal cord compression - LMN at lesion - UMN below lesion - Leg weakness - Urinary incontinence retention - Sensory level - In acute injury there may initially be LMN signs Cauda equina sydrome - LMN - Perianal anaesthesia - Leg weakness - Bladder retention
61
Radiculopathy symptoms + signs
• Motor o LMN symptoms for the muscles innervated by this spinal root • Sensory o Dermatomal pattern o Pain, numbness
62
Spinal cord compression symptoms + signs
* Acute onset – trauma * Chronic onset – osteoporosis, tumours • Motor o Limb weakness (hemiplegia/paraplegia) o LMN symptoms at the level of the lesion o UMN symptoms below the level of the lesion • Sensory o Sensory loss below a specific level o Back pain • Autonomic o Constipation o Urinary incontinence/retention o Erectile dysfunction
63
Cauda equina symptoms
* LMN symptoms * Perianal anaesthesia * Bladder retention * Leg weakness
64
Cushing’s reflex/triad What is it sign of?
Bradycardia HTN Irregular breathing Sign of increased ICP
65
Mononuclear visual loss
optic nerve lesion
66
Homonymous hemianopoia
Lesion in the occipital lobe
67
Bitemporatal hemianopoia
Lesion in the optic chiasm
68
Fatiguability - where is the lesion
NMJ
69
Syringomyelia symptoms + signs
o Syrinx starts in cervical cord o Spinothalamic tract is affected – bilateral loss of pain + temperature along the back and arms o Dorsal roots not affected – vibration, proprioception, fine touch not affected o LMN signs at the level of the syrinx (arms) o UMN below the syrinx (legs) o Paralysis, weakness o MRI spine o If fluid cavity is in the brainstem – syringobulia  vocal cord paralysis, ipsilateral tongue wasting, trigeminal sensory loss
70
What is weird about myoclonic seizures?
o Pt often remains conscious + alert throughout | brief shock like jerk of a muscle or muslce groups
71
Complex partial seizures also called temporal lobe epilepsy describe
Focal seizures - Impairement of consciousness - Patient may still be awake - Aura (epigastric discomfort) - Automatisms (playing with fingers, lip smacking) - Hallucinations - Olfactory hallucinations - Abnormal posture may be adopted due to dystonia - Patient doesn't remember the events after the attack - often derived from temporal lobes
72
What are Jacksonian seizures?
Focal motor seizure Simple partial seizure spreads from the distal part of the limb to the rest of the ipsilateral side of the body Can lead to paralysis of involved limbs for several hours Subtype of SPS (simple partial seizure) Electrical activity causes a tingling sensation to march across a region of the body from one group of distal muscles to the other This is often accompanied by automatisms, muscle cramping, hallucinations, head turning
73
Spinal stenosis symptoms + signs
Spinal stenosis Pain relieved when sitting/leaning forwards Caused by narrowing of the spinal canal due to spondylosis Presents with: a)back pain + b) sciatica Pain worse when spine is extended  going downhill, walking Pain better when spine is flexed  going uphill, sitting
74
Lateral medullary syndrome symptoms + signs
* Ipsilateral sensory deficits of the face + CN * Contralateral sensory deficits of the trunk + the extremities * Sudden onset vomiting + vertigo * Diminished gag reflex * Palatal paralysis * Nystagmus * Horner’s syndrome * Broad based ataxic gait Caused by occlusion of the posterior inferior cerebelar artery
75
How does a head injury present?
Agitation Headaches Vomiting Dizziness
76
Which is most commonly affected in MS? cone cells or rod cells
Cone cells (colour vision + high acuity central vision) – myelinated, therefore more commonly affected Rod cells (dark vision + peripheral vision) – non-myelinated, less commonly affected
77
Difference between Essential tremor/familial tremor PD tremor Cerebellar tremor
Essential tremor/familial tremor Absent at rest Appear on action 6-12 Hz Fine amplitude May be ameliorated by alcohol or beta blockers No other parkinsonian symptoms are present PD tremor Present at rest, exacerbated by concentration Disappear on action 3-7 Hz Coarse amplitude Commonly affects the distal limbs asymmetrically Cerebellar tremor Increases in magnitude throughout the movement to be maximal on approaching the target 4-6 Hz Associated with other cerebellar signs (DANISH)
78
cavernous sinus pathology
complete ophthalmoplegia of the affected side + loss of forehead sensation on the affected side The cavernous sinuses of either side communicate with one another - thrombosis + fistula formation can cause symptoms on the other side as well
79
Damage in Wernicke’s area Broca’s area
Wernicke’s area – inability to understand language, able to produce fluent, non-sensical speech [Temporal lobe] Broca’s area – ability to understand language, inability to produce fluent speech (broken speech) [Frontal lobe]
80
Central pontine myelinolysis is a result of.... signs + symptoms
Raising the Na too quickly in a hyponatraemic patient Damage to the myelin sheath of the neurones that make up the pons Acute paralysis, dysarthria, dysphagia
81
Lumbar spinal stenosis what makes it worse what makes it better
pain in the lower limbs Worse when walking/standing for long periods of time Eased by bending forwards to widen the spinal canal
82
stroke affects _____ side of face | brainstem lesions affect _______ side of face
stroke affects contralateral side of face | brainstem lesions affect ipsilateral side of face
83
How do you elicit Hoffman's sign and what does it represent?
Positive Hoffman's sign Flick the distal phalanx of the middle finger - thumb contracts This indicates an UMN lesion
84
Cerebellar problem vs proprioceptive problem
Cerebellar problem - patients can't stand with their feet together even if their eyes are open Proprioceptive loss - patients can stand with their feet together if they have their eyes open but lose their balance once they close their eyes (positive Romberg's test)
85
What does the Romberg's test test?
Proprioception
86
Ventricular septal defect VSD symptoms + signs
Pansystolic murmur Cyanosis Clubbing Raised JVP often occurs
87
Haemorrhagic stroke presents...
Suddenly with a thunderclap headache
88
Lacunar strokes can present with
Unilateral motor disturbance affecting the face, arm or leg or all 3 Complete one sided sensory loss Ataxia hemiparesis