Patterns of Neurological Presentation Flashcards

1
Q

what type of movement disorders are caused by problems of the corticospinal / pyramidal tract?

A

pyramidal / UMN features

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

what type of movement disorders are caused by problems of the basal ganglia?

A

EXTRAPYRAMIDAL

hyperkinetic MD

  • dystonia
  • tics
  • myoclonus
  • chorea
  • tremor

hypokinetic (rigidity, bradykinesia)

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

what type of movement disorders are caused by problems of cerebellum?

A

ataxia

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

weakness may be focal or non-focal, what is the difference between these?

A

focal - in distribution of peripheral nerve or spinal root, hemi-distribution, pyramidal distribution

non-focal - generalised, predominantly proximal or distal, if truly generalised it includes bulbar motor function otherwise quadri or tetraparesis

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

in UMN lesion, what pattern of sensory loss is seen compared to LMN?

A

UMN - central pattern

LMN - none, glove, stocking, peripheral nerve or root distribution

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

what is the difference between deep tendon reflexes, superficial reflexes and pathological reflexes in UMN lesion vs LMN?

A

UMN - increased deep tendon, decreased superficial and increased pathological

LMN - normal or decreased deep tendon, normal superficial and pathological

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

how is the sphincter function affected in UMN lesion vs LMN?

A

UMN = sometimes impaired

LMN = usually normal (unless for example cauda equina lesion)

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

how is muscle tone and bulk affected in UMN and LMN lesions?

A

UMN = increased tone, sometimes muscle hypertrophy

LMN = normal / decreased tone, muscle wasting

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

what are the main upper motor neurone signs?

A
increased tone 
hyper-reflexia 
extensor plantar responses
spastic gait 
exaggerated jaw-jerk
slowed movements
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what are the main lower motor neurone signs?

A

muscle wasting
weakness
fasciculations
absent or reduced deep tendon reflexes

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

what is an upper motor neurone pattern of weakness?

A

increased tone
brisk reflexes
pyramidal / corticospinal pattern of weakness (weak extensors in arm, weak flexors in legs)

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

what is a lower motor neurone pattern of weakness?

A

wasting, fasciculation, decreased tone, decreased or absent reflexes, flexor plantars (normal)

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

what are the signs of muscle disease?

A

wasting (usually proximal), decreased tone, decreased or absent tendon reflexes

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

what are the signs of neuromuscular junction disease?

A

fatiguable weakness, normal or decreased tone, normal tendon reflexes
no sensory symptoms

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

what are the signs of functional weakness?

A

no wasting, normal tone, normal reflexes, erratic power, non-anatomical loss

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

UML pattern of weakness usually occurs with stroke, SOLs and spinal cord problems and can usually be determined by body segments involved and accompanying signs - what signs suggest a hemispheric, parasagittal frontal lobe and spinal cord lesion?

A

hemispheric = contralateral pyramidal weakness in face, arm and leg

parasagittal frontal lobe lesion = paraparesis

spinal cord = pyramidal weakness below level of lesion (cervical = arms and legs, thoracolumbar = legs)

17
Q

what conditions can cause lower motor neurone pattern of weakness?

A

motor neurone disease

spinal muscular atrophy (lead poisoning, poliomyelitis)

18
Q

how does peripheral nerve involvement normally present?

A

symmetrical polyneuropathy with weakness and sensory symptoms (diabetes, alcohol, metabolic insults)
mononeuropathy (nerve compression) or mononeuritis multiplex (asymmetric polyneuropathy) which occurs in diabetes or vasculitis

19
Q

give examples of conditions which are neuromuscular junction disorders?

A

myasthenia gravis
organophosphate poisoning
lambert-eaton paraneoplastic syndrome

20
Q

what are the different patterns of sensory loss and what type of disorder do these indicate?

A

stocking - length dependent neuropathy
sensory level - spinal cord lesion
haemianaesthesia - contralateral cerebral lesion
dissociated sensory loss with lost spinothalamic but preserved dorsal column - hemicord damage

21
Q

what are the signs of a cerebellar disorder?

A

gait - broad based and unsteady
intention tremor / ataxia (assessed by finger-nose test and knee-heel test)
dysdiadochokinesis - clumsy fast alternating movements
nystagmus and dysarthria are additional features

22
Q

what is the role of the frontal lobe?

A

generates novel strategies and has executive functions

enables self criticism and trying again

23
Q

what are the many signs which can be associated with frontal lobe dysfunction?

A
personality dysfunction 
paraparesis 
paratonia 
grasp reflex
frontal gait dysfunction (magnetic gait)
cortical hand 
seizures
incontinence 
visual field defects
expressive dysphasia (brocas area)
anosmia
24
Q

what are the signs of temporal lobe dysfunction?

A

memory dysfunction (esp episodic memory)
agnosia (visual and sensory modalities in particular)
language disorders (wernickes)
visual field defects (congruous upper homonymous quadrantanopia)
auditory dysfunction (heschel’s gyrus)
limbic dysfunction
temporal lobe epilepsy

25
Q

what are the signs of parietal lobe dysfunction?

A

visual field defect (congruous lower homonymous quadrantanopia)
sensory dysfunction (visual and sensory modalities)
gerstmanns syndrome (disease of dominant angular gyrus - dysgraphia, left-right disorientation, finger agnosia, acalculia)
dyspraxia
inattention
denial

26
Q

what are the symptoms of a lacunar stroke?

A

no visual field defect
no new higher cortical or brainstem dysfunction

pure motor hemiparesis or pure sensory deficit of one side of the body, or sensorimotor hemiparesis or ataxia hemiparesis (dysarthric clumsy hand syndrome or ipsilateral ataxia with crural hemiparesis)

at least 2 of the 3 areas (face, arm and leg) should be involved

27
Q

what are the symptoms of posterior circulation stroke?

A

one of:

  • cranial nerve palsy
  • unilateral or bilateral motor or sensory deficit
  • disorder of conjugate eye movements
  • cerebellar dysfunction
  • homonymous hemianopia
  • cortical blindness
28
Q

what are the symptoms of total anterior circulation stroke?

A

hemiplegia and homonymous hemianopia contralateral to lesion
AND
either aphasia or visuospatial disturbances
+/- sensory deficit contralateral to the lesion

29
Q

what are the symptoms of partial anterior circulation syndrome?

A

one or more of unilateral motor or sensory deficit, aphasia or visuospatial neglect (with or without homonymous hemianopia)

motor or sensory deficit may be less extensive than in lacunar syndromes