NEURO WK 3 Flashcards

(30 cards)

1
Q

MND

A

motor neurone disease
degenerative
weakness, older men

riluzole

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

what symptom is one of the main causes of death in MND??

A

RESPIRATORY FAILURE

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

Subtypes of MND (umbrella term) and what is the most common ?? **

A

ALS - most common, upper and lower
Progressive Bulbar palsy
PLS - upper
PMA - lower

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

RED FLAG SIGNS OF RESPIRATORY FAILURE AND TREATMENT

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

upper motor signs vs. lower motor

A

upper - hyperreflexia, hypertonia, spasticity

lower - hyporreflexia, hypotonia, muscle wasting and fasciculations (twitching)

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

condition affecting the NEUROMUSCULAR JUNCTION

A

MG

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

clinical features of MG

A

tiredness

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

Presynaptic issues (2) - RARE

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

postsynaptic issues - MORE COMMON

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

diagnostic test for MG, and treatments for MG

what is associated with MG

A
  • anti-AChR IgG** in serum (elisa test)
  • Repetitive nerve stimulation - gradually reducing responses indicates NMJ dysfunction

ACh inhibitor - pyridostigmine
steroids
Thymectomy - association w thymoma

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

WHAT DRUGS TO AVOID IN MG

A

antibiotics

fluoroquinolone antibiotics (e.g., ciprofloxacin, levofloxacin)

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

examination of muscle and power grading

A

EMG

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

most common muscular dystrophy??

A

duchenne’s

gower’s sign

x-linked recessive

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

Be aware of treatable muscle disorders – polymyositis, dermatomyositis and rhabdomyolysis

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

myotonia

A

delayed relaxation of muscles after voluntary contraction or after a mechanical stimulus

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

rhabdomyolysis triad !!!

A

elderly man collapsed on ground and can’t get up

muscle pain/weakness
dark urine
decreased urine output

17
Q

Understand the differences between peripheral neuropathy, radiculopathy, mononeuropathy and mononeuritis multiplex. Where are the nerves damaged??

18
Q

GBS

A

ascending weakness
Campylobacter illness
glove and stocking distribution

IvIg and plasmapheresis

19
Q

Understand the difference between axonal and demyelinating neuropathies

A

AXONAL - affecting the axon

eg. diabetes

DEMYELINATING - affecting the myelin sheath eg. MS, GBS

20
Q

acute vs chronic demyelinating neuropathies

A

acute - GBS

chronic - MS

21
Q

Differentiate between small and large fibre neuropathies - large fibre motor, large fibre sensory, small fibre, autonomic. symptoms, power, sensation and reflexes

22
Q

KNOW THE DIFFERENT PATTERNS OF SENSORY LOSS

A

central loss

glove and stocking

23
Q

What is Parkinson’s ?? main cause? triad

A

loss of dopaminergic neurones in the substantia nigra

rigidity, bradykinesia and resting tremor

24
Q

PATHOLOGICAL HALLMARK OF PD

A

presence of Lewy bodies in certain regions of the brain, alpha synuclein
protein

25
Ix and Mx of Parkinson's
DaTscan (SPECT imaging) MRI/CT scan of head levodopa
26
PARKINSON-PLUS SYNDROMES
MSA PSP DLB
27
T1, T2
28
definition of sleep
reversible loss of consciousness and reduced responsiveness to the surrounding environment.
29
stages of sleep
non REM REM
30
what are the 2 peaks of drowsiness / peak patterns?
2pm-4pm early morning